GB822090A - New sulphonyl-ureas and process for their manufacture - Google Patents

New sulphonyl-ureas and process for their manufacture

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Publication number
GB822090A
GB822090A GB16825/57A GB1682557A GB822090A GB 822090 A GB822090 A GB 822090A GB 16825/57 A GB16825/57 A GB 16825/57A GB 1682557 A GB1682557 A GB 1682557A GB 822090 A GB822090 A GB 822090A
Authority
GB
United Kingdom
Prior art keywords
cyclohexyl
methoxypropyl
methylbutyl
hydrocarbon radical
sulphonyl
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
GB16825/57A
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
Application filed by Hoechst AG, Farbwerke Hoechst AG filed Critical Hoechst AG
Publication of GB822090A publication Critical patent/GB822090A/en
Expired legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

The invention comprises sulphonyl ureas of the general formula R-SO2-NH-CO-NH-R1 wherein R is an aliphatic or cycloaliphatic hydrocarbon radical of 3 to 8 carbon atoms and R1 is a saturated or unsaturated cyclic or open chain aliphatic hydrocarbon radical interrupted by oxygen or sulphur, and salts of these compounds. The compounds are made by known methods for the preparation of sulphonyl ureas and especially by the methods described in the parent Specification. Examples describe the preparation of sulphonyl ureas of the above general formula in which R and R1 respectively have the values: 3-methylbutyl, 3-methoxypropyl; 3-methylbutyl, 3-ethoxypropyl; cyclohexyl, 2-methoxyethyl; cyclohexyl, 3-methoxypropyl; cyclohexyl, tetrahydrofurfuryl; cyclohexylmethyl, 3-methoxypropyl and cyclohexyl, 2-ethylthioethyl. N - (3 - Methyl - butane - (1) - sulphonyl) - carbamic acid methyl ester used as a starting material is made by reaction of 3-methylbutyl sulphonamide and methyl chloroformate in the presence of potassium carbonate. Specification 595,472 [Group IV], also is referred to.ALSO:Antidiabetic preparations for oral administration comprise sulphonamides of the formula R-SO2-NH-CO-NH-R1 wherein R is an aliphatic or cycloaliphatic hydrocarbon radical of 3-8 carbon atoms and R1 is a saturated or unsaturated cyclic or open-chain aliphatic hydrocarbon radical interrupted by oxygen or sulphur or salts thereof with phyisologically tolerable bases in admixture or conjunction with a pharmaceutical carrier. Sulphonamides are specified in which R and R1 respectively are 3-methylbutyl, 3-methoxy-propyl; 3-methylbutyl, 3-ethoxypropyl; cyclohexyl, 2-methoxyethyl; cyclohexyl, 3-methoxypropyl, cyclohexyl, tetrahydrofurfuryl; cyclohexylmethyl, 3-methoxypropyl and cyclohexyl, 2-ethylthioethyl.
GB16825/57A 1956-05-26 1957-05-27 New sulphonyl-ureas and process for their manufacture Expired GB822090A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE822090X 1956-05-26

Publications (1)

Publication Number Publication Date
GB822090A true GB822090A (en) 1959-10-21

Family

ID=6742122

Family Applications (1)

Application Number Title Priority Date Filing Date
GB16825/57A Expired GB822090A (en) 1956-05-26 1957-05-27 New sulphonyl-ureas and process for their manufacture

Country Status (1)

Country Link
GB (1) GB822090A (en)

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