NZ621615B2 - N-[5-(aminosulfonyl)-4-methyl-1,3-thiazol-2-yl]-n-methyl-2-[4-(2-pyridinyl)phenyl]acetamide mesylate monohydrate - Google Patents

Abstract

The present disclosure relates to an improved and shortened synthesis of N-[5- (aminosulfonyl)-4-methyl-1,3-thiazol-2-yl]-N-methyl-2-[4-(2-pyridinyl)phenyl]acet-amide and the mesylate monohydrate salt thereof by using boronic acid derivatives or borolane reagents while avoiding toxic organic tin compounds and to the mesylate monohydrate salt of N-[5-(aminosulfonyl)-4-methyl-1,3-thiazol-2-yl]-N- methyl-2-[4-(2-pyridinyl)phenyl]acet-amide which has demonstrated increased long term stability and release kinetics from pharmaceutical compositions. pounds and to the mesylate monohydrate salt of N-[5-(aminosulfonyl)-4-methyl-1,3-thiazol-2-yl]-N- methyl-2-[4-(2-pyridinyl)phenyl]acet-amide which has demonstrated increased long term stability and release kinetics from pharmaceutical compositions.

Description

N-[5-(Aminosulfonyl)methyI-1,3-thiazol-Z-yl]-N-methyl-2—[4—(2- pyridinyl)phenyl]acetamide mesylate monohydrate Specification The present ion relates to an improved synthesis of N-[5—(aminosulfonyl)—4- methyl-1 ,3—thiazolyl}-N-methyl[4-(2-pyridinyl)phenyl]acetamide and the mesylate monohydrate salt thereof by using boronic acid derivatives or borolane 1O reagents while avoiding toxic organic tin compounds and to the mesylate monohydrate salt of N—[5-(aminosulfonyl)methyl-1,3-thiazol—2—yl]—N-methyl[4—(2- pyridinyl)phenyl]acet—amide which has demonstrated increased long term stability and release kinetics from pharmaceutical compositions.

Background of the invention Synthesis of N-[5-(aminosulfonyl)methyl-1,3-thiazol—2—yl]—N—methyl~2—[4—(2— nyl)phenyl]acetamide is known from EP 1244641 B1, and the use of acidic components ing esulfonic acid for the formulation of tablets containing micronized N-[5-(aminosulfonyl)—4-methyl-1,3-thiazol-2—yl]-N-methy|—2— [4-(2—pyridinyl)phenyl]acetamide is disclosed by A1.

It is the objective of the present invention to provide an improved synthesis for the compound aminosulionyl)-4—methyl-1,3-thiazo|-2—y|]-N-methyl—2—[4-(2-pyridinyl) phenyl]acetamide and a stable salt which exhibits increased long term stability and improved release kinetics from pharmaceutical formulations as well as a pharmaceutical formulations comprising that salt with ed release kinetics.

The objective of the t invention is solved by the teaching of the independent claims. Further advantageous features, aspects and details of the invention are evident from the dependent claims, the ption, the figures, and the examples of the t application.

Description of the invention The present ion relates to an improved and novel sis of the pharmaceutically active compound N-[5-(aminosulfonyl)—4-methyl-1,3-thiazol-2—yl]- N—methyl—2—[4—(2—pyridinyl)phenyl]acetamide as well as its mesylate salt. This improved synthesis starts from the same compounds as the older known synthesis of the state of the art but combines three reaction steps by the use of a boronic acid derivatives or borolane reagent. This modification makes the complete synthesis easier by avoiding two separation and purification steps and is also able to increase the yield.

The older known synthesis as described in EP 1244641 B1 on page 21 starts from 2-bromopyridine. In step 1 the 2—trimethylstannanylpyridine is prepared in a 45 to 50% yield (of the theory). The ethylstannanylpyridine is subsequently reacted with ethyl (4—bromophenyl)acetate in order to obtain the ethyl (4-pyridin ylphenyl)acetate in a 75% yield. In the third step the ethyl (4—pyridin—2- 1O ylphenyl)acetate is saponified to the (4-pyridinylphenyl)acetic acid with about 95% yield of theory. Consequently, the state of the art synthesis as shown below \ Step1 Sn(CH3)3 \ Step 2, 75% | —>| | 45—50% ’N Step 3, NaOH/EtOH, 95% \ N comprises 3 steps with an over all yield of about 34% ing two tion and purification steps which take time and involve the use of solvents for extracting and g the desired compounds as well as arrangements for purifying them.

The synthesis of the present invention as shown below (30002H5 O‘B\ 5 Pd(OAC)2, PPhs, EtsN o + toluene, reflux #0O~B\ 1Step NaOH CI W0 I COOH /\ Z_ es the three discrete steps by using c acid derivatives or borolane or a borinane reagent which allows for synthesis of the key ediate (4—pyridin-2— ylphenyl)acetic acid in a single stage with an over all yield of about 40% of theory avoiding the two separation and purification steps of the state of the art synthesis.

As an added t, the use of boron containing reagents is advantageous over the use of the toxic organic tin compounds in that the resulting boric acid by— product can be easily removed by an s wash. In contrast, organic tin compounds are not only a known problem in process waste streams, but are also noted for notoriously inating the resulting products of the down—stream synthesis. The (4—pyridin-2—ylphenyl)acetic acid is reacted with 4—methyI (methyiamino)-1,3-thiazolesulfonamide to the final product which is then converted to the definite mesylate monohydrate salt as shown below.

COOH PHa (EH3 H—N N 7" N N oY// CH3 s / 043—, s / / \ N OjS\NHZ \ N 4IS\NH2 o o/ EtOH H30803H C|H3 N N o f/ \ N 0’s $\H I,[\NHOI 2 H3C—SO3 * H20 Thus the present invention is directed to a method for synthesizing N—[5- (aminosulfonyl)—4-methyl-1 ,3-thiazo|-2—y|]-N—methyl[4-(2-pyridinyI)phenyl]acet- amide and the mesylate salt thereof according to the following steps: Step A: Reacting compound A of the following general formula A* COOR2 R1 represents a leaving group and R2 represents an alkyl residue with 1 to 6 carbon atoms or a cycloalkyl residue with 3 to 6 carbon atoms, with a boronic acid derivative, borolane, borinane or diboronic acid reagent under elimination of R1—H or R‘-B(OR)2 and formation of an intermediate c acid derivative of compound A, wherein preferred sts for the reaction are the reagent systems palladium acetate with triethylamine and triphenylphosphine or PdCl2(PPh3)2 with ylamine, wherein the intermediate boronic acid derivative is then reacted with the pyridine compound B of the following general formula 8* | 3* wherein R3 represents a leaving group under basic conditions in order to obtain the (4—pyridin—2—ylphenyl)acetic acid as an alkaline solution of the corresponding carboxylate salt.

The resulting (4-pyridin-2—yiphenyl)acetic acid was purified by simple washings at different pH and clear filtration steps ed by precipitation or crystallization, preferably by property adjusting the pH of an aqueous acidic solution of idin— 2—ylphenyl)acetic acid with an appropriate amount of base to 3.5 — 5.0, preferably 3.8 — 4.7. Beside the simple washing and filtration step, no further purification of the idin-2—ylphenyl)acetic acid or any of the intermediates by, for instance, recrystallization or chromatography is required.

Step B: Reacting (4-pyridin-2—ylphenyl)acetic acid ed from step A with 4-methyl-2—(methylamino)-i ,3—thiazolesulfonamide CH/3 weswfcm Cf \NH2 in order to obtain N-[S-(aminosu|fony|)methyI-1,3-thiazoIy|]-N-methyl-2—[4-(2— pyridinyl)phenyl]acetamide of the formula o sf \ 0"], \NH2S N The N-[5-(aminosulfonyI)—4-methyl—1,3—thiazo|—2-y|]-N—methyl[4-(2-pyridinyl)— phenyl]acetamide is fter most preferably converted (as step C) to the so far unknown monohydrate of the mesylate salt of aminosulfonyl)methyI—1,3- |y|]-N-methyl—2—[4—(2—pyridinyl)pheny|]acetamide. It has to be stated that a 1O mesylate salt is disclosed in A1 but not the specific mono mesylate drate salt which exhibits the improved properties.

The inventive method for synthesizing the N-[5-(aminosulfonyl)-4—methyl-1,3—thiazol- 2—y|]-N-methyl—2—[4—(2—pyridinyl)phenyl]-acetamide methanesulfonic acid mono- hydrate may further comprise step D directed to the preparation of a pharmaceutical composition of said methanesulfonic acid monohydrate salt: Step D: Preparing a pharmaceutical composition of the crystalline N-[S— (aminosulfonyl)methyl-1 ,3-thiazol—2-yI]—N-methyl[4-(2—pyridinyl)phenyl]— acetamide methanesulfonic acid monohydrate with at least one pharmaceutically acceptable carrier, excipient, solvent and/or diluent.

Such a pharmaceutical ition can be prepared by admixing or blending the crystalline N-[5-(aminosulfonyl)-4—methy|—1,3-thiazo|-2—yl]—N—methyl—2-[4-(2—pyridinyl) phenyl]-acetamide methanesulfonic acid monohydrate together with at least one ceutically acceptable carrier, excipient, solvent and/or diluent.

The inventive method may further comprise step E ing the step D: Step E: Adding salicylic acid, trifluridine, idoxuridine, foscarnet, cidofovir, ganciclovir, aciclovir, penciclovir, valaciclovir and/or famciclovir to the pharmaceutical composition of the lline N—[5-(aminosulfonyI)—4- methyl-1,3—thiazolyl]—N—methyl-2—[4-(2-pyridinyl)phenyI]-acetamide methanesulfonic acid monohydrate and at least one pharmaceutically acceptable carrier, excipient, solvent and/or diluent.

Thus after step E a pharmaceutical composition containing acetylsalicylic acid, trifluridine, idoxuridine, foscarnet, cidofovir, ganciclovir, aciclovir, penciclovir, valaciclovir or famciclovir or a pharmaceutical composition containing acetylsalicylic acid and trifluridine or acetylsalicylic acid and idoxuridine or salicylic acid and foscarnet or acetylsalicylic acid and cidofovir or acetylsalicylic acid and ganciclovir or acetylsalicylic acid and aciclovir or acetylsalicylic acid and penciclovir or acetylsalicylic acid and valaciclovir or acetylsalicylic acid and famciclovir in combination with crystalline N-[5- (aminosulfonyl)—4—methy|—1,3—thiazoly|]-N-methyl-2—[4-(2-pyridinyl)phenyl]— 1O acetamide methanesulfonic acid drate together with at least one pharmaceutically acceptable r, excipient, solvent and/or diluent is ed.

Consequently the present invention relates also to a pharmaceutical composition containing acetylsalicylic acid or aciclovir or penciclovir or salicylic acid and aciclovir or acetylsalicylic acid and penciclovir and crystalline aminosulfonyl)-4— methyl—1,3-thiazol-2—yl]-N-methyl[4-(2—pyridinyl)phenyl]-acetamide methanesulfonic acid monohydrate together with at least one pharmaceutically acceptable carrier, excipient, solvent and/or diluent. Some suppliers use the name acyclovir d of aciclovir.

The term "leaving group" as used herein is a molecular fragment that s with a pair of electrons in heterolytic bond cleavage Leaving groups can be anions or neutral molecules. Common anionic g groups are halides such as Cl", Br", and l‘, and sulfonate esters, such as para-toluenesulfonate ("tosylate", TsO'), trifluoromethanesulfonate ("triflate", TfO'] CF3SOQO—), benzenesulfonate late, CeHsSogo') or methanesulfonate ("mesylate", MsO‘).

General formula A* as shown below covers all phenyl acetic acid esters having a leaving group on the phenyl residue in position 4.

Thus R1 preferably represents -F, —ct —Br, —I, —OMs, —OTf and —OTs. The group "—OMs" refers to —OMesylate, the group "—OTf" refers to —OTriflate and the group "—OTs" refers to -OTosylate.

The group R2 represents an alkyl residue with 1 to 6 carbon atoms or a cycloalkyl e with 3 to 6 carbon atoms, and preferably —CH3, —C2H5, —03H7, —CH(CH3)2, —C4Hg, —CH2—CH(CH3)2, 3)—02H5, —C(CH3)3, aCan, aCsH13, cyclo—03H5, cyclo-C4H7, cyclo-C5Hg, cyclo-CBHH‘ More preferred are 01 eCHg, —CzH5, —C3H7, —CH(CH3)2, "C4Hg, —CH2—CH(CH3)2, ~CH(CH3)—CgH5, )3, and —CsH11. Especially preferred are ‘CH3, —C2H5, —C3H7, and rCH(CH3)2A Various borolanes and borinanes as well as the ponding diboronic acid derivatives can be used in step A of the inventive synthesis sed herein.

Preferred are borolanes of the following general formula: R‘O/B\OR" wherein R’ and R" are independently of each other any substituted or unsubstituted, linear or branched alkyl group with 1 to 10 carbon atoms or cycloalkyl group with 3 to 10 carbon atoms, or R’ and R" can also form together with the boron atom a cyclic ring wherein R’ and R" together form a substituted or unsubstituted, linear or branched alkylen group with 2 to 10 carbon atoms. Preferably R' and R" 2O represent independently of each other —CH3, —02H5, —C3H7, —CH(CH3)2, *C4H9, —CH2—CH(CH3)2, —CH(CH3)~C2H5I —C(CH3)3‘ and —CsH11. The cyclic borolanes are preferred.

The followin- borolanes, borinanes and diboronic acid derivatives are oreferred: Catechol boran Diborolane Diborinane wherein R3, Rb, RC, Rd, Re and Rf represent independently of each other a substituted or unsubstituted, linear or branched alkyl group with 1 to 10 carbon atoms or cycloalkyl group with 3 to 10 carbon atoms. Preferred are the linear alkyl residues with 1 to 6 carbon atoms, and most red are —CH3, —C2H5, —C3H7 and —CH(CH3)2.

Especially preferred examples for the above borone containing compounds are 4,4,5,5-tetramethyl[1,3,2]dioxaborolane (pinacolborane), [1,3,2]dioxaborolane, [1 ,3,2]dioxaborinane, 5,5-dimethyl[1,3,2]dioxaborinane, 4,6,6—trimethyl[1,3,2]— 1O orinane, 4,4,6,6—tetramethyl[1,3,2]—dioxaborinane, 4,4,5,5,6,6- hexamethyl[1,3,2]—dioxaborinane, diisopropoxyborane, hexahydrobenzo[1,3,2]di— oxaborole, 9,9-dimethyl—3,5-dioxabora-tricyclo-[61.1.62'6]decane, 6,9,9- trimethyl—3,5-dioxa—4-bora—tricyclo[6.1.1.62'6]decane, i32Pin2 (bis(pinacolato)diborane), bis(neopentylglycolato)diboron and catecholboran.

In step A this boronic acid derivative, borolane, borinane or diboronic acid reagent is reacted with a compound A of general formula A* in order to obtain an intermediate borolan or borinane reagent which is not isolated and purified, This reaction may be ted by the use of either catalysts prepared in situ by combination of palladium salts such as [Pd(OAc)2] and PdCl2 with triphenylphosphine (PPh3), tri-ortho- hosphine (P(o-Tol)3), tricyclohexylphosphine (PCya), tri-tert-butylphosphine, 1,4-Bis-(diphenylphosphino)-butane (dppb), and is—(diphenylphosphino)- ferrocene dppf or preformed catalysts such as Pd(PPh3)2CI2, Pd(PPh3)4, Fibrecat 1032, and Pd(dppf)C|2 in the presence of a variety of organic and inorganic bases such as triethylamine (Et3N), NaOAc, KOAc, and K3PO4. For this on heating to ature between 70°C and 150°C, preferably between 80°C and 130°C, more preferably between 90°C and 110°C is preferred. Moreover aprotic and preferably apolar solvents and preferably ic solvents such as benzene or e or xylenes are used.

This step A improves the state of the art synthesis by avoiding the use of toxic organic tin compounds which are a big m in the purification of the waste streams as well as the actual product(s) of the reaction which are y drugs for use in humans.

The intermediate boronic acid reagent is subsequently reacted with a pyridinyl compound of the l formula 8*, wherein R3 represents a leaving group. Thus R3 represents —F, —Cl, —Br, —I, —OMs, —OTf and —OTS and preferably —C| or -Br.

The corresponding (4—pyridinylphenyl)acetic acid ester is in situ treated with an aqueous base in order to cleave the ester linkage. It could be ageous to heat the reaction mixture during the coupling / fication step to moderate ature and preferably to ature between 40°C and 90°C, more 01 preferably between 45°C and 80°C, still more preferably between 50°C and 70°C and most preferably between 55°C and 65°C.

After purification and isolation of the key intermediate idinylphenyl)acetic acid, the (4—pyridin-2—ylphenyl)acetic acid was obtained in a yield of at least 40% of theory including only one isolation and purification step.

Further advantages of the present method are: . Purification and Pd removal by successive washes of aqueous alkaline and acidic product solutions with organic solvents (toluene, MIBK, EtOAc, MeTHF etc).

. Additional Pd depletion by charcoal / Celite treatment.

. Crystallization is possible from either alkaline or acidic aqueous ons by neutralization (at preferably 50-70 °C) Thereafter the (4—pyridin-2—ylphenyl)acetic acid was reacted with 4-methyl-2— (methylamino)-1,3-thiazolesulfonamide of the formula which was prepared according to the synthesis disclosed in EP 1244641 B1 in order to obtain N—[S—(aminosulfonyl)-4—methyl-1,3—thiazo|—2—yl]HN-methyl—2—[4—(2— pyridinyl)pheny|]acetamide of the formula N /N o TfCHg / O’/IS\NH2 In WO 01/47904 A the amide coupling reaction is described using HOBT (1— Hydroxy-1H-benzotriazole hydrate) in DMF which — due to its explosive character — generally causes ms during up-scaling. In addition, during the zation s the solvent DMF had been detected as cause for a variety of by-products (from Vilsmaier type formylations). ts for improved coupling conditions resulted surprisingly in the successful use of EDC x HCI (1ethyl(3-dimethylaminopropy|)carbodiimide hydrochloride) without HOBT in NMPITHF t combinations. Thus Step B of the above— mentioned method is ably carried out with EDC x HCI as coupling agent (without HOBT) in THF I NMP solvent mixtures having a ratio of 10: 1 to 1:1. The following re-crystatlization from THF / water resulted in a depletion of Pd to < 5 ppm. A total yield of > 80% for coupling and recrystallization could be achieved.

Thus the present invention also relates to the compound N-[5-(aminosulfonyI) methyl-1,3-thiazol-2—yl]-N-methyl[4—(2—pyridinyl)pheny|]acetamide ed according to the synthesis as disclosed herein.

This N-[5-(aminosulfonyI)-4—methyl-1,3-thiazoIyI]-N-methyl-2—[4-(2-pyridinyl)- phenyl]acetamide was thereafter converted to the crystalline mesylate drate salt which was not disclosed in the state of the art so far. A not stoichiometric mesylate salt was already known in the state of the art, but not the definite and stoichiometric mono mesylate monohydrate salt having exactly one mol equivalent water and one mol equivalent mesylate per mol equivalent N—[5-(aminosulfonyl) methyl—1,3-thiazolyl]—N-methyl[4—(2-pyridinyl)-phenyl]acetamide.

Thus the present invention relates to the compound N-[5-(aminosulfonyl)methyl- 1,3—thiazol—2—yl]—N—methyl[4-(2—pyridinyl)—phenyl]acetamide methanesulfonic acid drate and especially to crystalline N-[5-(aminosulfonyl)—4—methyI—1,3—thiazol- 2—yl]—N-methyl—2—[4—(2—pyridinyI)—phenyl]acetamide methanesulfonic acid mono- hydrate as well as to crystalline N-[5-(aminosulfonyl)—4—methyl-1,3-thiazol-2—yl]-N- methy|[4-(2-pyridinyl)—phenyl]acetamide methanesulfonic acid monohydrate obtainable and obtained according to the synthesis as disclosed herein. The N-[5- (aminosulfonyl)—4-methyI-1 ,3-thiazolyl]-N-methyI[4-(2-pyridinyl)—phenyl]acet- amide methanesulfonic acid monohydrate is substantially pure (purity above 96 weight-%, preferably > 98 weight-% and more ably > 99 -%) and is the definite monohydrate, i.e. 1 mol N-[5—(aminosulfonyl)methyl-1,3—thiazol—2-y|]—N- methyl-2—[4-(2-pyridinyl)—phenyl]acetamide methanesutfonic acid monohydrate contains 1 mol water and 1 mol mesylate anion in a regular lline structure as shown in Figures 2 and 3.

The crystalline mesylate monohydrate satt of N—[5—(aminosulfonyl)methyl-1,3— thiazolyI]-N-methyl-2—[4—(2-pyridinyl)-phenyl]acetamide is formed from a supersaturated solution of N-[5-(aminosulfonyl)-4—methyl-1 azolyl1-N-methyl—2— [4—(2—pyridinyl)-phenyl]acetamide and methanesulfonic acid by crystallization under lled conditions. Preferred ions for the crystallization are the addition of methanesulfonic acid at elevated temperatures, and preferably between 30°C and 90°C, more preferably between 35°C and 80°C, still more preferably between 40°C and 70°C, still more preferably between 45°C and 60°C and most preferably at 50°C — 55°C to the mixture of an organic solvent and water containing N-[5- su|fony|)methyl-1 ,3-thiazoly|]-N-methyl[4-(2-pyridinyl)phenyl]acet- amide ng a supersaturated solution of the mesylate of aminosulfonyI) methyl-1,3-thiazo|-2—y|]-N-methyl-2—[4-(2—pyridinyl)phenyl]acetamide. Organic solvents which are miscible or ute with water are preferred such as MeOH, EtOH, n-PrOH, I-PrOH, acetonitrile, THF, acetone. Moreover it is preferred to add seed crystals of N-[5-(aminosulfonyl)-4—methyl-1,3-thiazoly|]-N-methyl[4-(2- pyridinyl)phenyl]acetamide methanesulfonic acid monohydrate to this supersaturated mixture also at elevated temperatures like 30°C to 90°C, ably 35°C to 80°C, more preferably 40°C to 70°C, still more preferably 45°C to 60°C and most preferably at 50°C — 55°C. Also moderate to slow stirring of this mixture and a slow cooling of this mixture to room temperature are preferred. Furthermore it is preferred to add the methanesulfonic acid over 5 to 15 minutes at the elevated temperature and to keep the ing mixture at this elevated temperature for 0.5 to hour and more preferably 1 to 2 hours after completion of the on of the methanesulfonic acid. The g to room temperature is performed within 1 to 5 hour and preferably 2 to 3 hours and the mixture is thereafter slowly stirred for preferably another hour at room temperature. Then the crystals are filtered off, washed with alcohol/water and preferably dried under vacuum at a temperature between 20°C and 60°C, preferably starting at 20°C and ending at 60°C.

The crystalline mesylate monohydrate salt of N-[5-(aminosuifonyI)—4—methyI-1,3- thiazol-2—yl]—N-methyl[4-(2-pyridinyl)phenyl]acetamide exhibits increased long term stability properties and a desired or improved release kinetic especially from pharmaceutical itions and thus allows the preparation of long term stable pharmaceutical compositions. The long term stability of the crystalline mono mesylate monohydrate salt of N-[5-(aminosulfony|)methyl-1,3-thiazoIyI]-N- methyl-2—[4-(2—pyridinyl)phenyl}acetamide is superior in comparison to the free base form of N-[5-(aminosulfonyl)methyI-1,3-thiazolyl]—N-methyI-2—[4-(2- pyridinyl)phenyl].

Moreover the crystalline mono mesylate drate salt of N-[5-(aminosulfonyl)—4- -1,3-thiazol—2-yl]—N—methyl[4—(2-pyridinyl)pheny|]acetamide exhibits also polymorphic stability in comparison to the free base form or other salts as evident from Table 1. Polymorphism refers to the ability of a solid material to exist in more than one crystal structure or solid form.

Table 1: Thermal analysis and polymorphic stability (Methods used: DSC, TGA) Thermal it ofh drate 1xHCI -—E§_| oss of water before melting 1stOH | 035 of water before meltin- 1szOH _"5 loss of water before meltin- Free Base 8.8% loss of water before melting TGA: Thermogravimetric Analysis or Thermal Gravimetric Analysis DSC: Differential ng Calorimetry Form: refers to the mono chloride salt, the mono mesylate salt, the mono tosylate salt and the free base of N—[5—(aminosuIfonyI)methyl-1,3-thiazoIy|]-N-methyl[4—(2— pyridinyl)pheny|]acetamide The free base form as well as the hydrochloride and te salts form hydrates of low thermal and low polymorphic stability. Upon mild heating (about 50°C to 60°C), the water t is reduced which would make these salts and the free base form extremely difficult to handle and to process during production and formulation. In contrast the hydrate of the mono mesylate salt is thermally stable and polymorphic stable at much higher atures of considerably above 100°C as judged by TGA.

The free base of N-[5-(aminosulfonyl)methyl—1,3-thiazoly|]-N-methy|—2—[4—(2— pyridinyl)—pheny|]acetamide exists in four polymorphic forms and an amorphous form at room temperature. In addition, l solvates can be detected for the free base ing on the solvent. The data currently available do not permit the identification of the thermodynamically most stable form because all batches synthesised according to prior art display more than one melting peak by differential scanning calorimetry. The physico—chemical properties of various salts (hydrochloride HCI, mesylate MsOH, tosylate TsOH) as well as of the free base have been investigated and compared (see Table 2).

Table 2. Salt screening for N-[5-(aminosulfonyl)methyI-1,3-thiazolyl]-N-methy|[4—(2- pyn‘dinyl)—pl1enyl]acetamide. n.a. not applicable, n.d. not determined, HPLC high re liquid chromato rahy, ++ ve oodlhigh +goodlhigh, -badllow, --ve bad/low. 1x Free Determined PhCOOH base by Preparation Final + and processing crystallisation Stirring for Stability to Ione week at dissociation room temperature HPLC: . 2 98%, Purity + + correct stoichiomet X-ray llinity + + diffraction, microscopy Water .. solubility 39.4 n.d 138.3 50 0 2 35:23g (mg/100 mL) . . Storage at stability to. ++ ++ ++ 90 °C for one decomposmon. week Dihydrochloride (2xHCI), dimesylate (2stOH), ditosylate (2szOH) and benzoate (1xPhCOOH) salts of the free base of N-[5-(aminosulfonyl)—4—methyI-1,3-thiazoI—2- yl]-N-methyl[4—(2-pyridinyl)—phenyl]acetamide do not meet the criterion of stoichiometry. In addition, the hydrate of the monohydrochloride salt shows a decrease of crystallinity during e. rmore, the free base and the monotosylate form hydrates with low termal ity making them unsuitable for tabletting. These results are sed in Table 1 above, where the polymorphic instability of the hydrochloride salt, the tosylate salt and the free base form are discussed. Thus surprisingly only the inventive mono mesylate salt exhibited the ed poiymorphic and thermal stabiliy in order to allow manufacture, processing and formulation especially in a pharmaceutical scale.

One possibility to e the crystalline N-[5-(aminosu|fony|)—4-methyi-1,3-thiazol-2— yl]-N-methyl[4-(2-pyridinyl)-phenyl]acetamide methanesulfonic acid monohydrate was by dissolving the base in 10 vol ethanol 1 water (1 :1 ), adding 1.15 equivalents of methanesulfonic acid at 50 — 55 °C during 5 — 15 min, g with 0.5 mol % of final product, ageing for 1 — 1.5 h at 50°C and cooling to 20 — 25°C during 2.5h.

After further stirring for 1h, the crystalline mesylate monohydrate was isolated by filtration and dried in vacuo, resulting in a yield of > 95%. Using this procedure, N- [5-(aminosulfony|)methyl-1,3—thiazol—2-y|]-N-methy|—2—[4-(2-pyridinyI)-phenyl]acet- amide methanesulfonic acid drate in purity >99% containing < 2ppm residual Pd could be prepared reproducibly concerning yield and purity.

Further, the crystalline N-[5-(aminosulfonyl)—4—methyl—1,3—thiazol—2—yl]—N-methyl[4- (2-pyridinyl)-phenyl]acetamide esulfonic acid monohydrate can be ed in a defined and stable polymorphic form and in on the co—precipitation of the less soluble free base form is avoided applying this s. Consequently the lline mesylate monohydrate of the present invention is free or substantially free of free base. 1O The inventive crystalline mesylate monohydrate salt further shows stability (as pure API and in pharmaceutical formulations) in long term stability studies, exhibits increased release kinetics from pharmaceutical compositions and leads to improved bioavailability.

As evident from figure 2 which shows the single-crystal X-ray structure analysis of the N-[5-(aminosulfonyl)—4—methyI-1,3-thiazoIyl]-N—methyl-2—[4—(2—pyridinyl)pheny|]— acetamide esulfonic acid monohydrate, the salt is formed between the mesylate and the protonated pyridinyl ring. Moreover, exactly one mol equivalent water is incorporated into the crystal structure wherein the hydrogen atoms of the water molecule form hydrogen bridges with oxygen atoms of two different mesylate molecules. This efined position in the crystal lattice (see figure 3) is verified by the fact that water is released from the crystal only at high temperature, starting at 160°C. Thus the inventive compound is a definite mono mesylate and mono hydrtate of aminosu|fonyl)methyl-1,3-thiazolyl]-N-methyl[4-(2—pyridinyl)- phenyI]—acetamide.

The crystalline N—[5—(aminosulfonyl)methyl-1,3-thiazolyl]-N—methyl—2—[4—(2— pyridinyl)—phenyl]acetamide methanesulfonic acid monohydrate according to the ion is a useful compound for the preparation of a pharmaceutical composition for treatment and/or prophylaxis of herpes virus infections and/or prevention of transmission of a herpes virus or herpes viruses. Pharmacokinetic data derived from single and multiple dose applications in healthy volunteers exhibited favourable plasma concentration over time profiles with long lasting half lives indicative for an once daily dosing regimen or less frequent such as once weelky. The plasma concentrations in humans exceeded those reached in in vivo and in vitro experiments sufficient to ively treat herpes simplex virus infections in various animal models and to prevent viral replication in cell culture.

Surprisingly it was found that crystalline N-[5-(aminosulfonyl)methy|—1,3—thiazoI yI]—N-methyl-2—[4-(2—pyridinyl)-pheny|]acetamide methanesulfonic acid monohydrate is highly active t herpes viruses and infections caused by herpes viruses, mainly herpes simplex viruses. Therefore the inventive lline N—[5— (aminosulfonyI)—4-methyl—1 ,3—thiazol-2—yI]-N—methyl[4-(2-pyridinyI)-pheny|]acet— amide methanesulfonic acid monohydrate is ally useful for the ent andlor prophylaxis of diseases, which are caused by herpes simplex viruses, and/or tion of ission of a herpes virus or herpes viruses. 1O Infections with herpes simplex viruses (HSV, subtype 1 and 2) are categorized into one of several distinct disorders based on the site of infection. Orofacial herpes virus ion, the visible symptoms of which are colloquially called cold sores or fever blisters, infects the face and mouth. Orofacial herpes is the most common form of infection. Genital herpes is the second common form of a herpes simplex virus infection. Although genital herpes is largely believed to be caused by HSV-2 only, genital HSV-1 infections are increasing, Other ers such as herpetic whitlow, herpes gladiatorum, ocular herpes (keratitis), cerebral herpes infection encephalitis, Mollaret's meningitis, neonatal herpes, and possibly Bell's palsy are also caused by herpes simplex viruses.

Further, the present invention relates to crystalline N-[5-(aminosulfonyl)methyl— 1,3-thiazoIyI]-N-methyl[4-(2-pyridinyl)-phenyl]acetamide methanesulfonic acid monohydrate in ation with an anti-inflammatory agent. Especially preferred is a combination of crystalline N—[5-(aminosu|fony|)methyl-1,3-thiazoI—2-yI]-N- methyl[4—(2—pyridinyI)-phenyl]acetamide methanesulfonic acid monohydrate and salicylic acid.

Furthermore, the present invention relates to crystalline N-[5-(aminosulfonyl)—4— methyl-1,3—thiazolyl]-N-methyl[4-(2—pyridinyl)-phenyl]acetamide methane- sulfonic acid monohydrate in combination with an anti-viral agent. The further anti- viral agent is preferably an antimetabolite and most preferably a nucleobase analogues, nucleotide analogues or nucleoside analogue drug. It is further preferred if the further anti—viral agent is useful against herpes viruses and/or against transmission of a herpes virus or herpes viruses and is selected from the group of drugs comprising but not limited to or consisting of: trifluridine, idoxuridine, net, vir, ganciclovir, aciclovir or penciclovir or the respective prodrugs valaciclovir or famciclovir. Most preferred is a combination of lline N-[5-(aminosulfony|)—4-methyl-1,3-thiazo|y|]-N-methyl[4-(2-pyridinyl)- phenyl]—acetamide methanesulfonic acid monohydrate and aciclovir or penciclovir or the respective prodrugs valaciclovir and famciclovir.

The combination of crystalline N—[5—(aminosulfonyl)-4—methyl-1,3-thiazol—2—yl]—N- methyl[4—(2—pyridinyl)—phenyl]acetamide methanesulfonic acid monohydrate and a further active agent (like anti—inflammatory, immunomodulatory, or anti-viral agents, e.g. therapeutic vaccines, siRNAs, antisense oligonucleotides, nanoparticles or virus uptake inhibitors such as n—docosanol) may be administered simultaneously in one single pharmaceutical composition or in more than one pharmaceutical composition, wherein each composition comprises at least one active agent.

The inventive compound is preferably used for the production of a pharmaceutical composition containing crystalline N-[5-(aminosulfonyl)—4—methyl—1,3—thiazolyl]—N- methyl—2—[4-(2—pyridinyl)phenyl]acetamide methanesulfonic acid monohydrate together with at least one pharmaceutically acceptable carrier, excipient, solvent and/or diluent. The crystalline N-[5-(aminosulfonyl)—4—methy|—1,3—thiazolyI]-N— methyl—2—[4—(2—pyridinyl)phenyl]acetamide methanesulfonic acid monohydrate used is free or substantially free of the free base form of N-[5—(aminosulfonyl)—4-methyl-1,3— lyl]—N-methyl-2—[4-(2—pyridinyl)phenyl]aoetamide.

The pharmaceutical compositions of the present invention can be prepared in a conventional solid or liquid carrier or ts and a tional pharmaceutically- made adjuvant at suitable dosage level in a known way. red preparations may be adapted for oral ation. These administration forms include, for example, pills, tablets, film tablets, coated tablets, capsules, mal formulations, micro- and nano-fon’nulations, s and deposits.

The pharmaceutical compositions according to the invention preferably ses 5 to 70% more preferably 10 to 30% by weight crystalline N-[5v(aminosulfonyl)41— —1,3—thiazol—2—yl]—N—methyl-2—[4-(2—pyridinyl)—phenyl]acetamide e— sulfonic acid monohydrate (all tage data are tages by weight based on the weight of the pharmaceutical preparations). The pharmaceutical composition comprises usually 2 to 600 mg of crystalline N—[5-(aminosulfonylH— methyl-1,3—thiazol-2—yl]-N—methyl-2—[4-(2—pyridinyl)—phenyl]acetamide methane— sulfonic acid monohydrate, preferably 5 to 500 mg, more preferably 10 to 300 mg and particularly preferably 20 to 200 mg based on a single dosage. The pharmaceutical composition according to the ion optionally comprises one or more filler which are for example selected from the group consisting of: microcrystalline cellulose, fiber cellulose, calcium phosphates and mannitol.

Preferably according to the invention microcrystalline cellulose and mannitol is used. The pharmaceutical composition expediently comprises 20 to 80%, preferably 40 to 80%, particularly preferably 45 to 70% microcrystalline cellulose and 1 to 40%, preferably 5 to 30%, particularly preferably 10 to 20% mannitol.

The pharmaceutical preparation according to the invention may comprise at least one disintegration auxiliary which is for e selected from the group consisting of starch, pre—gelatinized starch, starch glycolates, cross-linked polyvinylpyrrolidone, sodium carboxymethylcellulose (=croscarmellose sodium) 1O and other salts of carboxymethylcellulose. A e of two disintegration agents can also be used. According to the ion the use of croscarmellose sodium is red. The pharmaceutical composition expediently comprises 3 to 35%, preferably 5 to 30% and ularly preferably 5 to 10% of the disintegration auxiliary(ies). The pharmaceutical preparation of the invention may comprise at least one lubricant selected from the group consisting of fatty acids and their salts.

According to the ion the use of magnesium stearate is particularly preferred.

The pharmaceutical composition of the invention may comprise a flow agent which could be colloidas anhydrous silica or talcum powder. According to the invention 2O the use of Colloidas anhydrous silica is particularly preferred. The flow agent is expediently used in an amount of 0.3 to 20%, particularly preferably from 0.4 to 1.5% and most preferably from 0.5 to 1%.

A particularly preferred pharmaceutical composition of the invention ses: 5% — 30% crystalline aminosulfonyl)methyl-1,3—thiazol-2—yl]-N-methyl—2-[4- (2—pyridinyl)phenyl]acetamide methane-sulfonic acid monohydrate, 5% — 10% croscarmellose-sodium, 0.5 — 0.7% magnesium stearate, 40% — 70% micro— crystalline cellulose, 10% — 20% mannitol and 0.5% — 1% colloidal ous silica.

The pharmaceutical compositions according to the ion can be administered to a patient in need thereof once daily at a once daily dose of about 20 to 750 mg of crystalline N-[5—(aminosulfonyl)—4-methy|—1,3-thiazolyl]-N-methyi-2—[4-(2— pyridinyl)—phenyl]acetamide methanesulfonic acid monohydrate. The pharmaceutical compositions according to the invention can also be administered to a patient in need thereof thrice daily, twice daily, once daily, thrice weekly, twice weekly, or once weekly. The administration on a thrice weekly, twice , or once weekly basis is red and especially preferred is a once weekly administration, i.e. an administration one time a week of a pharmaceutical ition containing between 400 mg to 600 mg of the inventive N—[5- sulfonyl)—4-methyl-1,3-thiazo|yl]-N-methyl[4—(2—pyridinyl)-phenyl]acet— amide methanesulfonic acid monohydrate. Moreover it is preferred to start the administration of the mesylate monohydrate of the present invention with a high loading dose, for instance, with an initial single dose of 400 mg to 800 mg and to continue the administration with a lower dose of 100 mg to 150 mg per day or per week over the period of ent.

Furthermore, the present invention also es pharmaceutical compositions for the preferred parenteral application. Further ways of administration are dermal, ermal, intragastral, intracutan, intravasal, intravenous, intramuscular, intraperitoneal, intranasal, intravaginal, intrabuccal, percutan, , subcutaneous, sublingual, topical, or transdermal application. The stered pharmaceutical compositions contain in addition to typical vehicles and/or diluents crystalline N-[5—(aminosulfonyl)—4—methyl-1,3-thiazo|—2—y|]-N—methyI—2—[4—(2—pyridinyl)— phenyl]acetamide esulfonic acid monohydrate as active ingredient.

Further preferred are topical formulations of lline 2O N—[5-(aminosulfonyl)—4— methyl—1,3—thiazol-2—yl]—N-methyl[4-(2-pyridinyl)-phenyl]acetamide methane— sulfonic acid monohydrate for dermal or transdermal application. Preferred topical formulations are skin creams, skin lotions, emulsions, gels, suspensions, ointments, oils, lip sticks and balms.

The formulation may be added any conventional carriers, adjuvants and optionally other ingredients. Preferred auxiliaries originate from the group comprising or ting of: preservatives, antioxidants, stabilizers, solubilizers and odors.

Ointments, pastes, creams and gels may include at least one conventional carriers, for example animal and vegetable fats, waxes, paraffins, starch, tragacanth, cellulose derivatives, hylene glycols, silicones, bentonites, c acid, talc and zinc oxide or mixtures of these substances. Solutions and emulsions may include conventional carriers such as solvents, solubilizing agents and fiers, e.g. water, ethanol, isopropanol, ethyl ate, ethyl e, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3—butyl glycol, oils, particularly cottonseed oil, peanut oil, corn oil, olive oil, castor oil and sesame oil, glycerol fatty acid esters, polyethylene glycols and fatty acid esters of sorbitan or mixtures of these substances. Suspensions may include conventional carriers such as liquid diluents, for example water, ethanol or propylene glycol, suspending agents, e.g. ethoxylated isostearyl alcohols, polyoxyethylene and polyoxyethylene sorbitan esters, microcrystalline cellulose, bentonite, agar-agar and tragacanth or mixtures of these substances.

An inventive composition may contain lipid particles in which crystalline N—[5- (aminosulfonylH—methyl-t ,3-thiazol-2—yl]—N-methyl-2—[4—(2-pyridinyl)—phenyl]acet— amide methanesulfonic acid monohydrate is transported. The ation of the pharmaceutical composition may also contain nts, which are usually used in this type of composition, such as thickeners, ents, humectants, surfactants, 1O emulsifiers, preservatives, anti—foaming, perfumes, waxes, lanolin, propellants and dyes.

The inventive ceutical composition may also be present as an alcoholic gel which comprises crystalline N-[5-(aminosulfonyl)—4—methyl-1,3—thiazol-2—yl]-N— methyl-2—[4—(2—pyridinyl)—phenyl]acetamide methanesulfonic acid monohydrate and one or more lower ls or lower polyols, such as ethanol, propylene glycol or glycerol, and a ning agent, such as siliceous earth. The oily—alcoholic gels also comprise natural or synthetic oil or wax. Gels may also contain organic thickeners, such as Gum arabic, n gum, sodium alginate, ose derivatives, preferably methylcellulose, hydroxymethylcellulose, hydroxyethyl- cellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose or inorganic thickeners, such as aluminum silicates such as bentonite or a mixture of polyethylene glycol and polyethylene glycol stearate or rate.

An inventive pharmaceutical composition may contain the following preservatives: phenoxyethanol, formaldehyde on, parabens, pentanediol or sorbic acid.

As pharmaceutically acceptable carrier, excipient and/or diluents can be used carriers such as preferably an inert carrier like lactose, starch, sucrose, cellulose, magnesium stearate, dicalcium phosphate, calcium sulfate, talc, mannitol, ethyl l d filled capsules); suitable binders include starch, gelatin, natural sugars, corn sweeteners, natural and synthetic gums such as acacia, sodium alginate, ymethylcellulose, polyethylene glycol and waxes, sugars such as sucrose, starches derived from wheat corn rice and potato, natural gums such as acacia, gelatin and tragacanth, derivatives of seaweed such as alginic acid, sodium alginate and ammonium calcium alginate, cellulose materials such as cellulose, sodium carboxymethylcellulose and hydroxypropylmethyl- cellulose, polyvinylpyrrolidone, and inorganic compounds such as magnesium aluminum te; lubricants such as boric acid, sodium benzoate, sodium acetate, sodium chloride, magnesium stearate, m stearate, or potassium stearate, stearic acid, high melting point waxes, and other water soluble lubricants such as sodium chloride, sodium benzoate, sodium acetate, sodium oleate, polyethylene glycols and D,L-Ieucine; disintegrating agents (disintegrates) such as starch, methylcellulose, guar gum, modified starches such as sodium carboxymethyl starch, natural and synthetic gums such as locust bean, karaya, guar, tragaoanth and agar, ose derivatives such as methylcellulose and sodium carboxymethylcellulose, microcrystalline celluloses, and linked micro— crystalline celluloses such as sodium croscaramellose, alginates such as alginic 1D acid and sodium te, clays such as bentonites, and effervescent mixtures; coloring agents, ning agents, flavoring agents, preservatives; ts are for e silicon dioxide and talc; suitable adsorbent are clay, aluminum oxide, suitable diluents are water or water/propylene glycol solutions for parenteral injections, juice, sugars such as lactose, sucrose, mannitol, and sorbitol, starches d from wheat, corn rice, and potato, and celluloses such as microcrystalline cellulose.

The following es are included to demonstrate preferred embodiments of the invention. It should be appreciated by those of skill in the art that the techniques disclosed in the examples which follow represent techniques discovered by the inventor to function well in the practice of the invention, and thus can be considered to constitute preferred modes for its practice. However, those of skill in the art should, in light of the present disclosure, appreciate that many changes can be made in the specific embodiments which are disclosed and still obtain a like or similar result without departing from the spirit and scope of the invention.

Further modifications and ative embodiments of various s of the invention will be apparent to those skilled in the art in view of this description.

Accordingly, this description is to be construed as illustrative only and is for the purpose of ng those skilled in the art the general manner of carrying out the invention. It is to be understood that the forms of the invention shown and described herein are to be taken as examples of embodiments. ts and materials may be substituted for those illustrated and described herein, parts and processes may be reversed, and n features of the invention may be utilized ndently, all as would be apparent to one skilled in the art after having the benefit of this description of the invention. Changes may be made in the elements described herein without departing from the spirit and scope of the invention as bed in the following claims.

EXAMPLES Definition: As used herein, the term "1 vol." refers to 1 L per kg of the respective starting material (1 vol. = 1 L per kg of the respective material or starting material).

Example 1: Synthesis of N-[5—(aminosulfonyl)-4—methyl-1,3—thiazoI—2—yl]—N—methyI [4-(2-pyridinyl)-phenyl]acetamide methanesulfonate monohydrate Step 1 (Suzuki-Miyaura coupling and saponification) The inertized reactor is charged with bis(triphenylphosphine)palladium(lI) chloride (0.010 eq.) and reinertized. Then, toluene (1.65 vol.) is added. After heating to 40°C, triethylamine (3.00 eq.) is added. A solution of ethyl—4—bromophenylacetate (1.00 eq.) in toluene (0.82 vol.) is added. The resulting suspension is heated to 90-95°C prior to dosing pinacol borane (1.30 eq.) over a period of 60-90 min.

Stirring at 90-95°C is continued for at least 2 more h before conversion is checked by HPLC. After cooling to 10°C, 2-chloropyridine (1.00 eq.) is charged to the 2O reaction mixture. Then, 30% NaOH (6.00 eq.) is added followed by g to 55- 60°C. Stirring at this temperature is continued for at least 4 h before conversion is checked by HPLC. Once conversion is deemed complete, the reaction mixture is concentrated at about 300 mbar until 0.8 vol. of distillate have been collected.

The reaction mixture is diluted with water (2.72 vol), cooled to 20°C and the phases are separated. The organic layer is ded while the pH of the aqueous layer is adjusted to pH 1 by addition of 33% HCl at 20°C. MIBK (2.30 vol.) and Celite (165 g/kg) are added and the resulting mixture is stirred for at least min at 20°C before the solids are removed by filtration. The reactor and the filter cake are rinsed successively with water and the combined te is erred back into the reactor. The phases are separated and the aqueous layer is washed twice more with MIBK. After on with water, the aqueous acidic product solution was heated to 55°C and filtered through a plug packed with Celite at the bottom and ted charcoal on top. The Celite/charcoal plug was washed once more with pre—heated water (0.5 vol, 55°C) and the combined filtrate was charged back into the reactor. At 20°C, the pH was adjusted to ~30 by addition of 30% NaOH before the t solution was heated to 60°C. More NaOH was dosed to adjust the pH to 4.1-4.3. The ing suspension was stirred for 1—1.5 h at 60°C prior to being cooled to 20°C. After onal stirring for at least 1 h at this temperature, the product was filtered, washed twice with water, pre-dried in a flow of N2 and finally dried in vacuo at 50-65°C. Typical yield: 38-42%.

Step 2 (amide coupling) The reactor is charged with product from step 1 (1.00 eq.) and 4—methyl-2— (methylamino)-1,3—thiazole-5—sulfonamide (1.02 eq.). THF (708 vol.) and NMP (1.11 vol.) are added. The resulting suspension is cooled to 0°C prior to adding 1- 3—(3—dimethyllaminopropyl)carbodiimide hydrochloride (1.23 eq.) in 4 equal 1O portions over a period of > 90 min. After at least 2 more h at 0°C, the reaction e is warmed to 20°C. At this temperature, stirring is continued for additional 2 h before conversion is checked by HPLC. Then, at 10—15°C about 2% (0.2 vol.) of the reaction mixture are added to water (12.3 vol) within at least 5 min. The resulting thin sion is stirred at 10-15°C for at least 1 h prior to dosage of the remaining bulk of the on mixture over > 4 h. Stirring at 10—15°C is continued for at least 0.5 h before the solids are filtered off, washed with water and dried on a nutsche filter in a steady flow of N2 until deemed sufficiently dry (LOD < 45 % w/w; LOD: Loss on drying), The feed reactor is charged with the crude product, THF (8.15 vol), and water (up 2O to 1.17 vol. depending on LOD of crude t). The resulting suspension is heated to 60-65°C and stirred for 1 h at this temperature. An almost clear solution is obtained which is subjected to polish filtration using a heatable tense filter heated to 60°C. The feed reactor, the transfer lines and the filter are successively rinsed with a mixture of THF (044 vol.) and purified water (0.06 vol.) at 6065°C.

The combined filtrate is collected in a separate reactor and heated to C.

To the reactor content, water (3.23 vol.) is dosed over at least 30 min. Stirring at 50—55°C is continued for 1-1.5 h before r portion of water (8.93 vol.) is slowly added within 2 h. After stirring for 1—1.5 h at 50°C, the resulting suspension is cooled to 5°C over 2.5 h and stirred for further 0.5 h. Then, the solids are filtered off, washed with water (3 x 2.96 vol.) and pre—dried on the nutsche filter in a steady flow of N2. Final drying is accomplished in vacuo at 50—65°C using a conical drier. Typical yield: 78-83%.

Step 3 (Salt Formation) The reactor is d with product from step 2 (1.00 eq.), ethanol (4.96 vol.) and water (4.96 vol). After heating the resulting suspension to 50—55°C, methanesulfonic acid (1.15 eq.) is added within < 15 min. Complete ution of starting materials is typically observed at the very end of addition. Immediately within the next 5 min, stirring is reduced to the minimum acceptable rate and the on mixture is seeded with N-[5-(aminosu|fonyi)—4-methyl-1,3-thiazol—2—y|]-N- methyl-2—[4—(2—pyridinyI)-phenyl]acetamide methanesulfonate drate (0.005 eq.) which was ed in the desired polymorphic form in a preceding experiment. Slow stirring at 50-55°C is continued for 60-90 min prior to cooling to -25°C during > 2.5 h. After stirring for 1 more h, the solids are filtered off, washed with ethanol/water 5:2 VN (3.10 vol), pre-dried in a nitrogen flow and erred into a conical drier for final drying in vacuo at 20—60°C.

Typical yield: >95%.

Example 2: Tablet comprising 60 mg of N-[5-(aminosu|fonyl)-4—methyl—1,3—thiazoIyI]-N- methyl—2—[4—(2—pyridinyl)—phenyl]acetamide (calculated as free base form) according to the invention as micronized active compound, t of active compound about 59% (based on an unvarnished tablet): crystalline N-[5—(aminosulfonyl)—4-m ethyl-1 ,3-thiazolyl]— N-methyl[4—(2—pyridinyl)—phenyl]acetamide methanesulfonic acid monohydrate, 77.0 mg Avicel PH 101 118.0 mg Lactose, fine 40.0 mg Ac-Di-Sol 20.0 mg Polyinylpyrrolidone 25 10.0 mg Magnesium stearate 2.0 mg Example 3: Ointment comprising 30 mg of N-[5-(aminosuIfonyl)-4—methyI—1,3—thiazol—2—yI]—N— methyl-2—[4-(2—pyridinyl)—phenyl]acetamide (calculated as free base form) according to the invention as micronized active compound crystalline aminosutfonyl)4—methyl-1,3—thiazol-2—yl]- yI-Z-[4-(2—pyridinyl)—phenyl]acetamide methanesulfonic acid monohydrate, micronized 38.4 mg zinc oxide 60.0 mg talcum 60.0 mg glycerol 120.0 mg propyleneglycole 40.0 mg sterile water 80.0 mg Example 4: Gel comprising 40 mg of N-[5-(aminosulfonyl)methyI-‘|,3-thiazoI-2—yl]-N-methyl pyridinyl)—phenyl]acetamide (calculated as free base form) according to the invention as ized active compound. 1O crystalline N~[5-(aminosulfonyl)-4—methyl-1,3-thiazol—2-y|]- N—methyl—2—[4—(2—pyridinyl)—pheny|]acetamide methanesulfonic acid monohydrate, micronized 51.2 mg solution of sodium hydroxide 30.0 mg 1,2—propandiol 80.0 mg glycerol 20.0 mg polyacrylic acid 60.0 mg e water 280.0 mg Example 5: Gel comprising 40 mg of N-[5-(aminosulfonyl)methy|—1,3-thiazol-2—yl]—N—methyl-2— [4—(2—pyridinyl)—pheny|]acetamide (calculated as free base form) according to the invention as micronized active compound. crystalline aminosulfonyl)-4—methyl-1,3-thiazoIyl]— N-methyl-2—[4-(2—pyridinyl)—phenyl]acetamide methanesulfonic acid monohydrate, micronized 51.2 mg 1,2-propandiol 80.0 mg glycerol 20.0 mg 3O polyacrylic acid 60.0 mg e water 280.0 mg Example 6: Tablet comprising 50 mg of N-[5—(aminosu|fony|)-4—methyl—1,3—thiazol—2—yl]—N— methyl—2—[4—(2—pyridinyl)-pheny|]acetamide (calculated as free base form) according to the invention as micronized active compound, content of active compound about 59% (based on an unvarnished tablet): crystalline N-[5—(aminosulfonyl)—4—methyl-1,3—thiazoIy|]- N-methyI[4-(2-pyridinyl)—phenyl}acetamide methanesulfonic acid drate, micronized 64.00 mg Polyinylpyrrolidone 25 3.50 mg Microcrystalline cellulose 20.00 mg Croscamellose sodium 10.00 mg Magnesium stearate 0.85 mg optionally HPMC film coating 3.00 mg Example 7: Crystal structure of N—[5—(aminosulfonyI)—4—methyI-1,3-thiazo|—2-y|]-N—methyl[4—(2- ny|)pheny|]acetamide methanesuifonic acid monohydrate Formula C19H24N4O733, M = 516.62, F(000) = 540, colorless plate, size 0.02 - 0.13 ' 0.15 mm3, triclinic, space group P -1 Z = 2, a = 9.4908(7)A, b = 9.5545(7) A, c = 14.4137(9) A, o = 86.130(3)°, [3 = 72.104(3)°, y = 68.253(4)°, V = 1153.68(15) A3, Deals, = 1.487 Mg ms. The crystal was measured 2O on a Nonius CD diffractometer at 293K using graphite-monochromated Mo Ka—radiation with A = 0.71073 A, em = 30.065°. Minimal/maximal transmission 095/099, (1 = 0.370 mm'1. The COLLECT suite has been used for datacollection and integration. From a total of 43492 reflections, 6761 were independent (merging r = 0.026). From these, 4955 were considered as observed (l>3.00(|)) and were used to refine 298 parameters. The structure was solved by direct methods using the program SlR92. Least-squares refinement t F was carried out on all non—hydrogen atoms using the program LS. R = 0.0313 (observed data), wR = 0.0432 (all data), GOF = 1.0736. Minimal/maximal al on density = 028/033 e A'3. Chebychev mial weights were used to complete the refinement.

Single-crystal structure parameters for N-[5—(aminosulfonyIH-methyI-1,3—thiazoI—2— yI]—N—methyl[4—(2—pyridinyl)pheny|]acetamide methanesutfonic acid monohydrate are shown in Figure 1 A.

Characteristic peaks of batch BXR3NCi obtained by X—ray powder diffraction analysis are shown in Table 3.

Table 3: Characteristic peaks of batch BXR3NC1 obtained by X-ray powder ction analysis (Cu Kalpha ation). (2-Theta °) (1 ngstrom) The 2-Theta values are rounded to 1 decimal place due to a normal deviation of +/- 0.1 ° Example 8: The exposure of rats to N-[5-(aminosulfonyl)—4—methyI—1,3-thiazoly|]-N—methy|—2— [4-(2-pyridinyl)phenyl]acetamide in a repeated dose 13-week toxicity study 1O med with the free base N-[5-(aminosulfony|)—4-methyl-1,3-thiazoI—2-y|}-N- methyl[4-(2-pyridinyi)phenyl]acetamide (free base) was compared to the res observed in a 26-week repeated dose toxicity study performed with the mesylate monohydrate. In both studies, the test items were administered as 0.5% (w/v) tylose suspensions, and the concentrations were adjusted to the equivalents of free base N-[5-(aminosulfonyI)methyl-1,3-thiazo|y|]-N-methyl-2—[4—(2— pyridinyl)phenyl]acetamide.

Exposures were comparable after administration of 10, 50 and 250 mg/kg/day both after administration of the first dose (days ‘I, 2; Table 4), as well as after repeated dose administration for 13 weeks (Table 5). There was an indication of a ly higher exposure after a dose of 10 mg/kg/day. Of note was the observation that exposures after administration of N-[5—(aminosulfonyl)methy|- iazo|yl]-N-methyl[4—(2-pyridinyl)phenyllacetamide mesylate monohydrate were higher, after doses of 50 and 250 mg/kg/day (adjusted to the equivalents of free base), as compared to exposures after administration of the free base. The extent of re increased by up to 27-fold for Cmax and 4-fold for AUC. It is ded that N-[5-(aminosulfonyl)methy|—1,3-thiazol—2—y|]—N-methy|—2-[4—(2- pyridiny|)phenyl]acetamide mesylate monohydrate gave rise to higher exposures as compared to those observed following administration of equimolecular doses (50 and 250 mg/kg/day) of free base equivalents of aminosulfonyl)—4—methyl— 1,3-thiazoIyl]-N-methyl[4—(2-pyridinyl)pheny|]acetamide. Such a major 1O increase in the extent of exposure is thus indicative of the mesylate salts improved physicochemical properties giving rise to a more favourable dissolution profile with concomitant increase in systemic exposure ve to that observed following administration of the freebase.

This enhancement in exposure, following administration of the mesylate salt, therefore means that a higher exposure to the active ingredient is achieved giving rise to a greater efficacy and higher viral resistance barrier, both regarded as an essential feature for the treatment of viral infections. The enhancement of both efficacy and resistance barrier are judged to be prime features associated with the te salt ation Table 4: Comparison of exposures in the 13—week toxicity (free base) and the 26- week toxicity (mesylate salt) studies in rats after one administration. M male, F female. Cmax is the maximal observed analyte concentration; AUC(o.24) is defined as the area under the analyte vs. time concentration up to 24 hours post dosing; calculated by linear up/ln down ion Free base rMesylate monohydrate Exposure ratio 13-week toxicity 26-week toxicity study 26-wts/13-wts. study (13-wts) s) day 1 Lday 1 Dose [mg/kg/day] Gender Cmax Aucflm, Cmax AUCum) Cmax AUCMQ [ng/ml] ml] [ng/ml] [ngxh/ml] 13300 87900 16935 118752 50 E30600 246000 70324 633522 .3— 250 E53900 567000 133775 1932721 15300 159000 17237 175125 50 -_fl 250 --_- Table 5: Comparison of exposures in the 13—week toxicity (free base) and the 26— week ty ate monohydrate salt) studies in rats in week 13. M male, F female. Cmax is the maximal observed analyte concentration; 24) is defined as the area under the analyte vs. time concentration up to 24 hours post dosing; calculated by linear up/In down summation Free base Mesylate monohydrate Exposure ratio 13-week toxicity 26-week toxicity study 26-wtsl13-wts study (13-wts) (26-wts) Dose [mg/kg/day] Cmax [ngxh/ml} [ng/ml] [ngxh/ml] 133000 21840 227165 1172000 Description of figures Figure 1 shows A) the single-crystal structure parameters for N-[5-(aminosulfonyI)-4— methyl—1,3-thiazol-2—yl]-N-methyl[4-(2-pyridinyl)phenyllacetamide methanesulfonic acid monohydrate (batch BXR3NCt), B) the X—ray powder diffraction spectrum of N—[5—(aminosulfonyI)—4- 1O methyl—1,3—thiazolyI]-N-methyl—2-[4-(2-pyridinyl)phenyl]acetamide methanesulfonic acid monohydrate (batch BXRSNC‘l) as calculated from single crystal data, and C) an overlay of the X—ray powder ction spectra of N—[5— (aminosulfonyl)—4-methy|—1 ,3—thiazo|—2—y|]—N—methyl—2—[4—(2- pyridinyl)phenyl]acetamide methanesulfonic acid monohydrate of batch BXRSNCl as measaured (blue line) and as calculated (red line).

D) Measured X—ray powder pattern of batch BXRBNCt Figure 2 shows the X—ray structure of the N-[5-(aminosulfonyl)-4—methy|—1,S—thiazol— 2-yl]—N—methyl-2—[4—(2-pyridinyl)phenyl]acetamide methanesulfonic acid monohydrate with indicated hydrogen bridges, It is shown that the nitrogen atom of the pyridinyl ring (right side bottom) is ated and that a hydrogen bridge is formed between the hydrogen, which protonates the pyridinyl ring en, and one oxygen of the mesylate anion, and that another en bridge is formed between another oxygen of the mesylate anion and the hydrogen of the water molecule while the other hydrogen of the water molecule forms a hydrogen bridge with the oxygen of another mesylate anion.

Figure 3 shows the singlecrystal X—ray ure is of the N-[5-(amino- sulfonyl)-4—methyl—1,3-thiazo|—2—y|]—N—methyl-2—[4—(2—pyridinyl)phenyl]acet- amide methanesulfonic acid monohydrate as g within the crystal. It is shown that the phenylpyridinyl ring systems are oriented in planes, which are parallel to each other.

Claims (1)

1.WHAT WE CLAIM IS: - 1. Method for sizing N-[5-(aminosulfonyl)methyl-1,3—thiazoIyl]-N- methyl—2—[4-(2-pyridiny|)phenyl]acetamide according to the following steps: Step A: Reacting compound A of the following general formula A* 000R2 wherein R1 represents a g group and R2 represents an alkyl residue with 1 to 6 carbon atoms or a cycloalkyl residue with 3 to 6 carbon atoms with a boronic acid derivative, borolane, borinane or diboronic acid reagent under elimination of R1~H or R1-B(OR)2 and formation of an intermediate boronic acid derivative of compound A, n the ediate boronic acid derivative is then reacted with the pyridine compound B of the following general formula 8* l 8* wherein R3 represents a leaving group under basic conditions in order to directly obtain (4—pyridin ylphenyl)acetic acid which is then purified. 08/04/16 Step B: Reacting (4-pyridin-2—ylpheny|)acetic acid obtained from step A with 4-methyl- 2-(methylamino)-1,3—thiazolesulfonamide S%\CH3 0”/S\NH2 in order to obtain N—[5-(aminosuIfonyl)methyl-1,3—thiazo|y|]-N-methyI[4- (2-pyridinyi)phenyl]acetamide of the formula (EH3 o S? \ N fls‘sz 2. Method according to claim 1 further sing step C: ting N—[5—(aminosulfonyl)methyl-1,3-thiazol—2-y|]—N—methyI-2—[4—(2- pyridinyl)phenyl]acetamide with methanesulfonic acid in a mixture of an organic solvent and water to crystalline N-[5-(aminosulfonyl)—4-methyl-1,3-thiazolyl]—N- methyl-2—[4—(2—pyridinyl)phenyl]acetamide methanesulfonic acid monohydrate of the formula 08/04/16 I 8%- ‘ \NHS \ N ®\H (g 2 ch—SO3 * H20 3. Method according to claim 1, wherein R1 and R3 are ndently of each other selected form —F, —Cl, —Br, —I, —OMs, —OTf and —OTs. 4. Method according to claim 1, wherein the boronic acid derivative, boroiane, borinane or diboronic acid reagent is selected from: R’, R”, Ra, Rb, RC, Rd, Re and Rf represent independently of each other a substituted or unsubstituted, linear or branched alkyl group with 1 to 10 carbon atoms or cycloalkyl group with 3 to 10 carbon atoms. 5. Method according to claim 1, wherein for the preparation of the intermediate boronic acid derivative or boroiane reagent, the reagents palladium e, triethylamine and triphenylphosphine or PdCi2(PPh3)2 and triethylamine are used. 08/04/16 7. Method according to claim 2, wherein the mixture of of N-[5- (aminosulfonyl)methyl—1 azol-2—yl]—N-methyl-2—[4—(2- pyridiny|)phenyl]acetamide in an organic solvent and water yields a supersaturated solution upon addition of methanesulfonic acid at elevated temperatures from which the N—[5—(aminosulfonyl)methyl-1,3—thiazol-2—yl]-N— methyl-2—[4—(2—pyridinyl)phenyl]-acetamide methanesulfonic acid monohydrate crystallizes after either extended stirring, seeding or cooling. 8. Method according to any one of claims 1 to 7 further comprising step D: Preparing a pharmaceutical ition of the lline N-[5- (aminosulfonyl)methyl-1 ,3—thiazo|-2—yl]-N-methyl—Z—[4—(2—pyridinyl)phenyl]- acetamide methanesulfonic acid monohydrate with at least one aceutically acceptable carrier, excipient, solvent and/or diluent. Dated this 8th day of April 2016 AiCuris GmbH & Co. KG Patent Attorneys for the Applicant PETER MAXWELL AND ASSOCIATES