GB1149391A - Benzenesulphonyl-ureas and process for their manufacture - Google Patents

Benzenesulphonyl-ureas and process for their manufacture

Info

Publication number
GB1149391A
GB1149391A GB33416/66A GB3341666A GB1149391A GB 1149391 A GB1149391 A GB 1149391A GB 33416/66 A GB33416/66 A GB 33416/66A GB 3341666 A GB3341666 A GB 3341666A GB 1149391 A GB1149391 A GB 1149391A
Authority
GB
United Kingdom
Prior art keywords
benzenesulphonyl
acid
benzamido
chloro
methoxy
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB33416/66A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hoechst AG
Original Assignee
Hoechst AG
Farbwerke Hoechst AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=7101195&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=GB1149391(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Hoechst AG, Farbwerke Hoechst AG filed Critical Hoechst AG
Publication of GB1149391A publication Critical patent/GB1149391A/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/64Sulfonylureas, e.g. glibenclamide, tolbutamide, chlorpropamide
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C303/00Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
    • C07C303/36Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
    • C07C303/40Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reactions not involving the formation of sulfonamide groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/50Compounds containing any of the groups, X being a hetero atom, Y being any atom
    • C07C311/52Y being a hetero atom
    • C07C311/54Y being a hetero atom either X or Y, but not both, being nitrogen atoms, e.g. N-sulfonylurea
    • C07C311/57Y being a hetero atom either X or Y, but not both, being nitrogen atoms, e.g. N-sulfonylurea having sulfur atoms of the sulfonylurea groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/58Y being a hetero atom either X or Y, but not both, being nitrogen atoms, e.g. N-sulfonylurea having sulfur atoms of the sulfonylurea groups bound to carbon atoms of six-membered aromatic rings having nitrogen atoms of the sulfonylurea groups bound to hydrogen atoms or to acyclic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D309/08Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D309/14Nitrogen atoms not forming part of a nitro radical
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/12Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14The ring being saturated

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Macromonomer-Based Addition Polymer (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

1,149,391. Benzenesulphonyl-ureas and process for their manufacture. FARBWERKE HOECHST A.G. 25 July, 1966 [27 July, 1965], No. 33416/66. Heading C2C. Novel compounds of the general formula and their physiologically tolerable salts with bases, for example sodium salts, wherein X represents a chlorine or bromine atom or a methyl group linked to the 4- or 5-position with respect to the carboxylic amide group, preferably a chlorine atom, and Y represents a hydrogen atom or a methyl group are prepared by one of the following methods: (a) Reacting a benzenesulphonyl-isocyanate, -carbamic acid ester, -thiolcarbamic acid ester, -urea, -semi-carbazide or -semicarbazone carrying the substituent of formula in the p-position with an amine carrying the substituent of Formula III or a salt thereof; (b) reacting a sulphonamide of the formula or a salt thereof with an isocyanate, carbamic acid ester, thiolcarbamic acid ester, carbamic acid halide or urea carrying the substituent of Formula III (c) hydrolysing a correspondingly substituted benzenesulphonyl-isourea ether, -isourea ester, -isothiourea ether, -parabanic acid or -haloformic acid amidine; (d) adding water on to a correspondingly substituted carbodiimide; (e) replacing the sulphur atom in a correspondingly substituted benzene-sulphonyl-thiourea by an oxygen atom; (f) hydrogenating a corresponding benzenesulphonyl-urea containing, in the molecule, an unsaturated linkage; and (g) introducing by acylation the radical of formula into a benzenesulphonyl-urea of the formula and, if desired, converting the resulting compound into a physiologically tolerable salt thereof by reaction with a base. N - [4 - (beta - <2 - methoxy 5 - chloro - benzamido > - ethyl) - benzenesulphonyl] - N<SP>1</SP> - acetylurea is prepared by acylation with acetic acid anhydride of the amine. N,N<SP>1</SP> - bis - 4 - [beta - < - 2 - methoxy - 5- chloro - benzamido > - ethyl) - benzenesulphonyl]- urea is prepared by treatment of the corresponding carbamic acid with ammonia in the presence of the corresponding sulphonamide. N - [4 - (beta - < 2 - methoxy - 5 - chloro - benzamido > - ethyl) - benzenesulphonyl] - 3 - cyclohexyl-parabanic acid is prepared by reaction of N - cyclohexyl - parabanic acid and 4 - (beta- [2 - methoxy - 5 - chloro - benzamido] - ethyl)- benzenesulphochloride. N - [4 - beta - < 2 - methoxy - 5 - chloro - benzamido > ethyl) - benzenesulphonyl] - N<SP>1</SP> - cyclohexyl-isothiourea methyl ether is prepared by reaction of cyclohexylamine and N<SP>1</SP>[4-(beta-<2- methoxy - 5 - chloro - benzamido > ethyl) - benzenesulphonyl] - imino - dithiocarbonic acid dimethyl ester which is itself prepared by reaction of dimethyl sulphate on the potassium salt of the corresponding dithiocarbonic acid. Pharmaceutical compositions in conventional form for oral or parenteral administration useful in treating diabetes comprise an above novel compound and a suitable pharmaceutical carrier.
GB33416/66A 1965-07-27 1966-07-25 Benzenesulphonyl-ureas and process for their manufacture Expired GB1149391A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF46721A DE1301812B (en) 1965-07-27 1965-07-27 Process for the preparation of benzenesulfonylureas

Publications (1)

Publication Number Publication Date
GB1149391A true GB1149391A (en) 1969-04-23

Family

ID=7101195

Family Applications (2)

Application Number Title Priority Date Filing Date
GB33285/66A Expired GB1153272A (en) 1965-07-27 1966-07-25 Benzenesulphonyl-Ureas and Process for their manufacture
GB33416/66A Expired GB1149391A (en) 1965-07-27 1966-07-25 Benzenesulphonyl-ureas and process for their manufacture

Family Applications Before (1)

Application Number Title Priority Date Filing Date
GB33285/66A Expired GB1153272A (en) 1965-07-27 1966-07-25 Benzenesulphonyl-Ureas and Process for their manufacture

Country Status (22)

Country Link
JP (1) JPS526985B1 (en)
AT (11) AT274838B (en)
BE (2) BE684654A (en)
BR (2) BR6681115D0 (en)
CH (1) CH478103A (en)
CY (2) CY534A (en)
DE (1) DE1301812B (en)
DK (2) DK117419B (en)
ES (15) ES329462A1 (en)
FI (1) FI45959C (en)
FR (1) FR5943M (en)
GB (2) GB1153272A (en)
IL (2) IL26016A (en)
IN (3) IN139503B (en)
IS (2) IS756B6 (en)
IT (2) IT1043760B (en)
LU (2) LU51617A1 (en)
MC (1) MC601A1 (en)
MY (2) MY7000111A (en)
NL (1) NL6610580A (en)
NO (2) NO121834B (en)
SE (1) SE328566B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1670901A1 (en) * 1967-08-09 1971-03-18 Hoechst Ag Process for the preparation of benzenesulfonylureas
DE3833439A1 (en) * 1988-10-01 1991-09-12 Hoechst Ag METHOD FOR MICRONIZING GLIBENCLAMIDE

Also Published As

Publication number Publication date
DK117419B (en) 1970-04-27
CH478103A (en) 1969-09-15
ES329462A1 (en) 1967-12-01
ES355478A1 (en) 1969-12-01
ES355480A1 (en) 1969-12-01
BR6681609D0 (en) 1973-12-27
BR6681115D0 (en) 1973-12-26
AT278032B (en) 1970-01-26
IL26194A (en) 1970-05-21
AT274842B (en) 1969-10-10
CY540A (en) 1970-05-22
ES344047A1 (en) 1968-12-16
IT1043761B (en) 1980-02-29
MY7000086A (en) 1970-12-31
IT1043760B (en) 1980-02-29
NL6610580A (en) 1967-01-30
ES355476A1 (en) 1969-12-01
ES344044A1 (en) 1968-12-16
ES344049A1 (en) 1969-05-16
AT279638B (en) 1970-03-10
AT275541B (en) 1969-10-27
ES344045A1 (en) 1968-11-16
BE684654A (en) 1967-01-27
IS1582A7 (en) 1967-01-28
ES344046A1 (en) 1969-05-01
AT279637B (en) 1970-03-10
IN139501B (en) 1976-06-26
DK123652B (en) 1972-07-17
AT274841B (en) 1969-10-10
FR5943M (en) 1968-04-08
ES344048A1 (en) 1970-02-01
BE684652A (en) 1967-01-27
LU51617A1 (en) 1968-03-14
AT274839B (en) 1969-10-10
IN139503B (en) 1976-06-26
DE1301812B (en) 1969-08-28
GB1153272A (en) 1969-05-29
ES355475A1 (en) 1969-12-01
IS822B6 (en) 1972-12-29
MC601A1 (en) 1967-03-21
ES355477A1 (en) 1969-12-01
IL26016A (en) 1970-08-19
AT278031B (en) 1970-01-26
FI45959C (en) 1972-11-10
LU51616A1 (en) 1968-03-14
ES355481A1 (en) 1970-03-01
AT274838B (en) 1969-10-10
AT274840B (en) 1969-10-10
AT274830B (en) 1969-10-10
MY7000111A (en) 1970-12-31
NO123569B (en) 1971-12-13
IN139506B (en) 1976-06-26
IS756B6 (en) 1970-11-23
ES355474A1 (en) 1969-12-01
IS1581A7 (en) 1967-01-28
FI45959B (en) 1972-07-31
CY534A (en) 1970-04-07
SE328566B (en) 1970-09-21
ES355479A1 (en) 1970-03-01
NO121834B (en) 1971-04-19
JPS526985B1 (en) 1977-02-26

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