GB988773A - Sulphonyl ureas - Google Patents

Sulphonyl ureas

Info

Publication number
GB988773A
GB988773A GB22481/61A GB2248161A GB988773A GB 988773 A GB988773 A GB 988773A GB 22481/61 A GB22481/61 A GB 22481/61A GB 2248161 A GB2248161 A GB 2248161A GB 988773 A GB988773 A GB 988773A
Authority
GB
United Kingdom
Prior art keywords
hydrindene
reacting
sulphonyl
chloride
butyl
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
GB22481/61A
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.)
Olin Corp
Original Assignee
Olin Corp
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 Olin Corp filed Critical Olin Corp
Publication of GB988773A publication Critical patent/GB988773A/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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

The invention comprises hydrindenesulphonylureas (indanesulphonylureas) of the formula <FORM:0988773/C2/1> and salts such as the alkali and alkaline earth metal salts thereof, wherein R is an alkyl e.g. methyl, ethyl, propyl, isopropyl, butyl, t-butyl or amyl, alkenyl e.g. allyl, cycloalkyl e.g. cyclobutyl, cyclopentyl or cyclohexyl, aryl e.g. naphthyl, phenyl or an aralkyl group e.g. a phenethyl or benzyl group. The compounds are made by (a) reacting a salt of the hydrindenesulphonamide, such as an alkali-metal or alkaline earth metal salt, with an isocyanate R.NCO or a corresponding carbamoyl chloride or urethane; (b) reacting a hydrindenesulphonamide with a chloroformic ester, phosgene or an unsubstituted urethane or urea and reacting the resulting product with a primary amine; (c) reacting a hydrindenesulphonamide with a substituted thiourea and either desulphurizing the product or converting it to the guanidine analogue by treatment with silver nitrate and subsequently hydrolysing with a base to the sulphonyl urea compound and (d) reacting a hydrindenesulphonyl chloride with an isourea alkyl ether and hydrolysing the product. Ethyl hydrindene-4-sulphonyl carbamate is made by reacting hydrindene-4-sulphonic acid with thionyl chloride, treating the resulting hydrindene-4-sulphonyl chloride with ammonia to give the sulphonamide and reacting this with ethyl chlorocarbonate. 1 - n - Butyl - 3 - (hydrindene - 4 - sulphonyl)-thiourea is made by reacting hydrindene-4-sulphonamide with 1-n-butyl-thoiurea. 1 - n - Propyl - 3 - (hydrindene - 4 - sulphonyl)-guanidine hydrochloride is made by treating hydrindene-4-sulphonyl chloride with n-propylguanidine. 1 - (Hydrindene - 5 - sulphonyl) urea is made by reacting hydrindene-5-sulphonamide and urea. Pharmaceutical preparations having hypoglycemic activity comprise the above compounds of the invention embodied in conventional dosage forms such as tablets or capsules.
GB22481/61A 1960-06-29 1961-06-21 Sulphonyl ureas Expired GB988773A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEC21809A DE1159937B (en) 1960-06-29 1960-06-29 Process for the preparation of hydrindene sulfonylureas

Publications (1)

Publication Number Publication Date
GB988773A true GB988773A (en) 1965-04-14

Family

ID=7017075

Family Applications (1)

Application Number Title Priority Date Filing Date
GB22481/61A Expired GB988773A (en) 1960-06-29 1961-06-21 Sulphonyl ureas

Country Status (6)

Country Link
CH (1) CH411849A (en)
DE (1) DE1159937B (en)
DK (1) DK104054C (en)
FR (1) FR1376M (en)
GB (1) GB988773A (en)
NL (2) NL266494A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102219718A (en) * 2010-04-19 2011-10-19 巨野金岭生物科技发展有限公司 New synthesis method for p-tolunesulfonyl carbamide

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1294957B (en) * 1966-07-02 1969-05-14 Boehringer & Soehne Gmbh Process for the preparation of hydrindene sulphonylureas and sulphonyl semicarbazides
US4845128A (en) * 1984-06-27 1989-07-04 Eli Lilly And Company N([(4-trifluoromethylphenyl)amino]carbonyl)benzene sulfonamides
US5260338A (en) * 1984-06-27 1993-11-09 Eli Lilly And Company Anti-tumor method and compounds
IL80032A (en) * 1985-09-23 1992-07-15 Lilly Co Eli Anti-tumor phenyl-aminocarbonylsulfonamides,their preparation and pharmaceutical compositions containing them
US5116874A (en) * 1985-09-23 1992-05-26 Eli Lilly And Company Anti-tumor method and compounds
ZA915371B (en) * 1990-07-17 1993-03-31 Lilly Co Eli Antitumor compositions and methods of treatment
US5216026A (en) * 1990-07-17 1993-06-01 Eli Lilly And Company Antitumor compositions and methods of treatment
US5262440A (en) * 1991-12-10 1993-11-16 Eli Lilly And Company Antitumor compositions and methods of treatment
US5234955A (en) * 1991-12-20 1993-08-10 Eli Lilly And Company Antitumor compositions and methods of treatment
CA2110524A1 (en) * 1992-12-10 1994-06-11 Gerald Burr Grindey Antitumor compositions and methods of treatment

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE965400C (en) * 1955-09-04 1957-06-06 Hoechst Ag Process for the preparation of benzenesulfonylureas

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102219718A (en) * 2010-04-19 2011-10-19 巨野金岭生物科技发展有限公司 New synthesis method for p-tolunesulfonyl carbamide

Also Published As

Publication number Publication date
CH411849A (en) 1966-04-30
FR1376M (en) 1962-06-25
NL108745C (en) 1964-05-16
DE1159937B (en) 1963-12-27
DK104054C (en) 1966-03-28
NL266494A (en) 1964-01-15

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