GB1476116A - Triazole derivatives and processes for the production thereof - Google Patents

Triazole derivatives and processes for the production thereof

Info

Publication number
GB1476116A
GB1476116A GB2461675A GB2461675A GB1476116A GB 1476116 A GB1476116 A GB 1476116A GB 2461675 A GB2461675 A GB 2461675A GB 2461675 A GB2461675 A GB 2461675A GB 1476116 A GB1476116 A GB 1476116A
Authority
GB
United Kingdom
Prior art keywords
formula
alkyl
compound
prepared
derivatives
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
GB2461675A
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.)
Novartis AG
Original Assignee
Ciba Geigy 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 Ciba Geigy AG filed Critical Ciba Geigy AG
Publication of GB1476116A publication Critical patent/GB1476116A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/08Antiepileptics; Anticonvulsants

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Neurology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

1476116 Triazole derivatives CIBA-GEIGY AG 9 June 1975 [14 June 1974] 24616/75 Heading C2C Novel compounds of Formula I wherein R 1 is H, C 1-7 alkyl, hydroxymethyl optionally etherified or esterified, formyl, carboxy optionally functionally modified, or aminomethyl optionally mono or disubstituted; B 2 is C 1-7 alkyl and R 3 is H or C 1-2 alkyl or NH 2 R 3 is a saturated monoheterocyclic ring and rings A and B may be substituted by halogen, CF 3 , NO 2 , C 1-7 alkyl or C 1-7 alkoxy and salts thereof are prepared by one of the following methods: (a) a reactive ester of a compound of Formula II is reacted with HNR 2 R 3 or an alkali metal derivative thereof; (b) a compound of Formula IV is reacted with formaldehyde or formic acid; (c) a compound of Formula V is oxidized; (d) a compound of Formula VI wherein R 6 is C 1-7 alkyl is treated with a base and optional conversion to a salt or a substituent group is converted to a derivative thereof by standard procedures. Reaction esters (mainly halides) of compounds of Formula II above are prepared by halogenation and optional conversion of functional groups to their derivatives. Intermediates of Formula V are prepared by NaBH 4 reduction of the ketones optionally followed by conversion of functional group to their derivatives. [2 - (Dimethylamino) - acetamido] - [2 - (ochlorobenzoyl) - 4 - chlorophenylazo] - malonic acid diethyl ester is prepared by reacting 2- amino - 2<SP>1</SP>,5 - dichlorobenzophenone which has been diazotized with [2-(dimethylamino)acetamido]-malonic acid diethyl ester. Pharmaceutical compositions in conventional forms for oral, rectal or parenteral administration and having anticonvulsant activity comprise an above novel compound and a carrier or diluent.
GB2461675A 1974-06-14 1975-06-09 Triazole derivatives and processes for the production thereof Expired GB1476116A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH817574A CH601264A5 (en) 1974-06-14 1974-06-14

Publications (1)

Publication Number Publication Date
GB1476116A true GB1476116A (en) 1977-06-10

Family

ID=4336312

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2461675A Expired GB1476116A (en) 1974-06-14 1975-06-09 Triazole derivatives and processes for the production thereof

Country Status (22)

Country Link
JP (3) JPS6028825B2 (en)
AT (2) AT345821B (en)
AU (1) AU496929B2 (en)
BE (1) BE830214A (en)
CA (1) CA1074313A (en)
CH (1) CH601264A5 (en)
CS (1) CS189712B2 (en)
DE (1) DE2525691A1 (en)
DK (1) DK227075A (en)
DO (1) DOP1980002934A (en)
ES (4) ES438481A1 (en)
FR (1) FR2274302A1 (en)
GB (1) GB1476116A (en)
GT (1) GT198066871A (en)
HK (1) HK49580A (en)
HU (1) HU172467B (en)
IE (1) IE41550B1 (en)
IL (1) IL47474A (en)
MY (1) MY8100158A (en)
NL (1) NL7507104A (en)
SE (1) SE426393B (en)
ZA (1) ZA753809B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113372215A (en) * 2021-05-20 2021-09-10 吉林大学 Novel esterification method for synthesizing p-halomethyl benzoate

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5855147B2 (en) * 1976-06-04 1983-12-08 塩野義製薬株式会社 benzophenone derivatives
CN118019742A (en) 2021-09-29 2024-05-10 豪夫迈·罗氏有限公司 Novel benzodiazepine derivatives as GABA Aγ1 PAM

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113372215A (en) * 2021-05-20 2021-09-10 吉林大学 Novel esterification method for synthesizing p-halomethyl benzoate
CN113372215B (en) * 2021-05-20 2024-05-24 吉林大学 Novel esterification method for synthesizing p-halomethyl benzoate

Also Published As

Publication number Publication date
CH601264A5 (en) 1978-06-30
NL7507104A (en) 1975-12-16
ES438481A1 (en) 1977-06-16
DOP1980002934A (en) 1986-02-14
ES454005A1 (en) 1977-11-16
FR2274302B1 (en) 1979-08-17
SE426393B (en) 1983-01-17
JPS5111768A (en) 1976-01-30
FR2274302A1 (en) 1976-01-09
GT198066871A (en) 1982-06-05
ES454008A1 (en) 1977-11-16
IL47474A (en) 1980-01-31
HK49580A (en) 1980-09-12
JPS617424B2 (en) 1986-03-06
BE830214A (en) 1975-12-15
ATA455875A (en) 1978-02-15
DK227075A (en) 1975-12-15
CS189712B2 (en) 1979-04-30
ATA498877A (en) 1978-02-15
JPS59130279A (en) 1984-07-26
IE41550L (en) 1975-12-14
HU172467B (en) 1978-09-28
AT345822B (en) 1978-10-10
ES454006A1 (en) 1977-11-16
AU8208275A (en) 1976-12-16
AT345821B (en) 1978-10-10
DE2525691A1 (en) 1976-01-02
SE7505952L (en) 1975-12-15
ZA753809B (en) 1976-05-26
IL47474A0 (en) 1975-08-31
IE41550B1 (en) 1980-01-30
CA1074313A (en) 1980-03-25
AU496929B2 (en) 1978-11-09
JPS59108770A (en) 1984-06-23
MY8100158A (en) 1981-12-31
JPS6028825B2 (en) 1985-07-06
JPS6021984B2 (en) 1985-05-30

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Legal Events

Date Code Title Description
PS Patent sealed [section 19, patents act 1949]
PCNP Patent ceased through non-payment of renewal fee