GB789788A - A method for the preparation of n-ú¯-butyl-n-(ú­-acetamido-benzene-sulfonyl)-urea - Google Patents

A method for the preparation of n-ú¯-butyl-n-(ú­-acetamido-benzene-sulfonyl)-urea

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Publication number
GB789788A
GB789788A GB16631/56A GB1663156A GB789788A GB 789788 A GB789788 A GB 789788A GB 16631/56 A GB16631/56 A GB 16631/56A GB 1663156 A GB1663156 A GB 1663156A GB 789788 A GB789788 A GB 789788A
Authority
GB
United Kingdom
Prior art keywords
urea
butyl
acetylsulphanilamide
salt
acetamidobenzenesulphonyl
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
GB16631/56A
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.)
Instituto de Angeli SpA
Original Assignee
Instituto de Angeli SpA
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 Instituto de Angeli SpA filed Critical Instituto de Angeli SpA
Publication of GB789788A publication Critical patent/GB789788A/en
Expired legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

N - n - Butyl - N1 - (p - acetamidobenzene sulphonyl)-urea is prepared by reacting n-butylcarbamyl chloride with an anhydrous inorganic or organic salt of N4-acetylsulphanilamide. The preferred salts are those of alkali metals and of tertiary organic bases, e.g. pyridine, and in the latter case the salt is preferably formed in situ. In examples: (1) N4-acetylsulphanilamide in anhydrous pyridine is treated with n-butylcarbamyl chloride and the mixture heated to 120-25 DEG C., yielding N-n-butyl-N1-(p - acetamidobenzenesulphonyl) - urea, purified by solution in aqueous sodium carbonate, reprecipitation with acid, and crystallization from aqueous alcohol; (2) the sodium salt of N4-acetylsulphanilamide is treated with n-butylcarbamyl chloride yielding N-n-butyl-N1-(p-acetamidobenzenesulphonyl)-urea which is purified as in (1). Subsequent saponification with boiling 10 per cent NaOH yields N-n-butyl-N1-sulphanilyl-urea.
GB16631/56A 1956-04-14 1956-05-29 A method for the preparation of n-ú¯-butyl-n-(ú­-acetamido-benzene-sulfonyl)-urea Expired GB789788A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IT789788X 1956-04-14

Publications (1)

Publication Number Publication Date
GB789788A true GB789788A (en) 1958-01-29

Family

ID=11316632

Family Applications (1)

Application Number Title Priority Date Filing Date
GB16631/56A Expired GB789788A (en) 1956-04-14 1956-05-29 A method for the preparation of n-ú¯-butyl-n-(ú­-acetamido-benzene-sulfonyl)-urea

Country Status (1)

Country Link
GB (1) GB789788A (en)

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