ES416167A1 - 3-amino-pyrazolones-5, processes for their manufacture and their use as medicines - Google Patents

3-amino-pyrazolones-5, processes for their manufacture and their use as medicines

Info

Publication number
ES416167A1
ES416167A1 ES416167A ES416167A ES416167A1 ES 416167 A1 ES416167 A1 ES 416167A1 ES 416167 A ES416167 A ES 416167A ES 416167 A ES416167 A ES 416167A ES 416167 A1 ES416167 A1 ES 416167A1
Authority
ES
Spain
Prior art keywords
group
alkyl
phenyl
formula
alkoxy
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
ES416167A
Other languages
Spanish (es)
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.)
Bayer AG
Original Assignee
Bayer 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
Application filed by Bayer AG filed Critical Bayer AG
Publication of ES416167A1 publication Critical patent/ES416167A1/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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
    • C07D231/44Oxygen and nitrogen or sulfur and nitrogen atoms
    • C07D231/52Oxygen atom in position 3 and nitrogen atom in position 5, or vice versa

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Procedure for the production of 3-aminopyrazolones- (5), of the formula **(See formula)** in which R represents a phenyl radical substituted by 1 to 2 substituents equal or different from the group consisting of alkyl, phenyl, trifluoromethoxy, nitro, cyano, carbonamido, sulfonamido, alkylamino, fluorine, bromine and iodine, with two substituents on the ring being Phenyl together eventually form a 5- to 7-membered saturated or unsaturated branched or unbranched isocyclic or heterocyclic ring capable of containing oxygen and/or sulfur atoms; or a phenyl radical substituted by a SOn-alkyl group (n = 0 to 2), an alkoxy group or the group -O- (CH2) n-N- (alkyl) 2 (n = 2 to 3); or a phenyl radical substituted by two equal substituents from the group consisting of alkoxy and trifluoromethyl; or a phenyl radical substituted by two different substituents from the group consisting of alkyl, phenyl, halogen, alkoxy, trifluoromethyl, trifluoromethoxy, alkylamino, cyano, carbonamido, sulfonamido, SOn-alkyl (n = 0 to 2) and nitro; or a phenyl radical substituted by three chlorine atoms; or a naphthyl radical substituted by 1 to 2 the same or different halogen atoms and/or alkyl, or an unsubstituted β-naphthyl, anthryl or phenanthril radical; characterized in that hydrazines of formula (II) are reacted R-CH2-NH-NH2 (II) in which R has the meaning defined above, with derivatives of acetic acid of formula (III) **(See formula)** where X is a hydroxy, alkoxy, aralkoxy, amino or alkylamino radical, Y'is hydrogen and Y''is nitrile or Y' and Y'' together represent the group **(See formula)** Y representing an alkoxy, aryloxy, aralkoxy, alkylmercapto or aralkylmercapto radical or the amino group, optionally after isolation of the intermediate amidrazones formed of the formula (IV) **(See formula)** in which X and R have the meanings indicated above, possibly in the presence of inert solvents and of basic or acid catalysts, such as alkali and alkaline earth hydroxides and carbonates or such as hydrohalic acids, sulfuric acid or sulfonic acids, at temperatures between 20º and 100ºC. (Machine-translation by Google Translate, not legally binding)
ES416167A 1972-06-23 1973-06-22 3-amino-pyrazolones-5, processes for their manufacture and their use as medicines Expired ES416167A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE2230792A DE2230792A1 (en) 1972-06-23 1972-06-23 3-AMINO-PYRAZOLONE- (5), METHOD FOR MANUFACTURING AND USING IT AS A MEDICINAL PRODUCT

Publications (1)

Publication Number Publication Date
ES416167A1 true ES416167A1 (en) 1976-03-01

Family

ID=5848604

Family Applications (1)

Application Number Title Priority Date Filing Date
ES416167A Expired ES416167A1 (en) 1972-06-23 1973-06-22 3-amino-pyrazolones-5, processes for their manufacture and their use as medicines

Country Status (29)

Country Link
JP (1) JPS4962463A (en)
KR (1) KR780000147B1 (en)
AR (1) AR205329A1 (en)
AT (1) AT323735B (en)
BE (1) BE801228A (en)
BG (1) BG22819A3 (en)
CA (1) CA1017752A (en)
CH (1) CH592632A5 (en)
DD (1) DD109874A5 (en)
DE (1) DE2230792A1 (en)
DK (1) DK133468C (en)
EG (1) EG11039A (en)
ES (1) ES416167A1 (en)
FR (1) FR2189072B1 (en)
GB (1) GB1391051A (en)
HK (1) HK11276A (en)
HU (1) HU168358B (en)
IE (1) IE37834B1 (en)
IL (1) IL42560A (en)
LU (1) LU67854A1 (en)
NL (1) NL7308575A (en)
NO (1) NO137196C (en)
OA (1) OA04432A (en)
PH (1) PH11606A (en)
PL (1) PL87665B1 (en)
RO (1) RO71819A (en)
SE (1) SE401181B (en)
SU (1) SU472503A3 (en)
ZA (1) ZA734244B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USRE30420E (en) * 1973-04-17 1980-10-21 Bayer Aktiengesellschaft Pyrazol-5-ones
DE2319278C2 (en) * 1973-04-17 1986-02-20 Bayer Ag, 5090 Leverkusen Pharmaceutical agent
DE3436383A1 (en) * 1984-10-04 1986-04-10 Bayer Ag, 5090 Leverkusen METHOD FOR PRODUCING PYRAZOLONE DERIVATIVES

Also Published As

Publication number Publication date
BG22819A3 (en) 1977-04-20
HU168358B (en) 1976-04-28
LU67854A1 (en) 1973-08-30
AU5705173A (en) 1974-12-19
IE37834B1 (en) 1977-10-26
IL42560A0 (en) 1973-08-29
IL42560A (en) 1977-05-31
CA1017752A (en) 1977-09-20
GB1391051A (en) 1975-04-16
DK133468C (en) 1976-10-18
PL87665B1 (en) 1976-07-31
KR780000147B1 (en) 1978-04-19
OA04432A (en) 1980-03-15
DK133468B (en) 1976-05-24
JPS4962463A (en) 1974-06-17
IE37834L (en) 1973-12-23
ZA734244B (en) 1974-06-26
FR2189072A1 (en) 1974-01-25
RO71819A (en) 1981-01-30
NO137196B (en) 1977-10-10
SU472503A3 (en) 1975-05-30
BE801228A (en) 1973-12-21
PH11606A (en) 1978-04-12
EG11039A (en) 1977-01-31
AR205329A1 (en) 1976-04-30
NO137196C (en) 1978-01-18
FR2189072B1 (en) 1977-09-09
DD109874A5 (en) 1974-11-20
NL7308575A (en) 1973-12-27
SE401181B (en) 1978-04-24
CH592632A5 (en) 1977-10-31
DE2230792A1 (en) 1974-01-17
HK11276A (en) 1976-03-12
AT323735B (en) 1975-07-25

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