JPS56140961A - Preparation of sulfonate of p-ethoxycarbonylphenyl epsilon-guanidinocaproate - Google Patents

Preparation of sulfonate of p-ethoxycarbonylphenyl epsilon-guanidinocaproate

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Publication number
JPS56140961A
JPS56140961A JP4443780A JP4443780A JPS56140961A JP S56140961 A JPS56140961 A JP S56140961A JP 4443780 A JP4443780 A JP 4443780A JP 4443780 A JP4443780 A JP 4443780A JP S56140961 A JPS56140961 A JP S56140961A
Authority
JP
Japan
Prior art keywords
formula
compound
sulfonyl chloride
sulfonate
acid
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.)
Pending
Application number
JP4443780A
Other languages
Japanese (ja)
Inventor
Kunio Takahashi
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.)
SHIRATORI SEIYAKU KK
Shiratori Pharmaceutical Co Ltd
Original Assignee
SHIRATORI SEIYAKU KK
Shiratori Pharmaceutical Co Ltd
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 SHIRATORI SEIYAKU KK, Shiratori Pharmaceutical Co Ltd filed Critical SHIRATORI SEIYAKU KK
Priority to JP4443780A priority Critical patent/JPS56140961A/en
Publication of JPS56140961A publication Critical patent/JPS56140961A/en
Pending legal-status Critical Current

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

Abstract

PURPOSE: To obtain the titled compound useful as anticallicrein agent in one stage in high yield, by reacting a specific compound with a sulfonyl chloride in the presence of an acid acceptor.
CONSTITUTION: A sulfonate of ε-guanidinocaproic acid expressed by formula II (R is p-methylphenyl, etc.) and ethyl p-hydroxybenzoate of formula III are dissolved in an intert solvent, e.g. DMF, and a sulfonyl chloride of formula IV and an acid acceptor are added thereto and reacted at room temperature for about 1hr to give a compound of formula I. The sulfonyl chloride is used in an amount equimolar or more with the compound of formula II. Pyridine, etc. may be preferred as the acid acceptor.
EFFECT: Expensive acid-resistant apparatuses are not required without causing pollution problems.
COPYRIGHT: (C)1981,JPO&Japio
JP4443780A 1980-04-04 1980-04-04 Preparation of sulfonate of p-ethoxycarbonylphenyl epsilon-guanidinocaproate Pending JPS56140961A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4443780A JPS56140961A (en) 1980-04-04 1980-04-04 Preparation of sulfonate of p-ethoxycarbonylphenyl epsilon-guanidinocaproate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4443780A JPS56140961A (en) 1980-04-04 1980-04-04 Preparation of sulfonate of p-ethoxycarbonylphenyl epsilon-guanidinocaproate

Publications (1)

Publication Number Publication Date
JPS56140961A true JPS56140961A (en) 1981-11-04

Family

ID=12691460

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4443780A Pending JPS56140961A (en) 1980-04-04 1980-04-04 Preparation of sulfonate of p-ethoxycarbonylphenyl epsilon-guanidinocaproate

Country Status (1)

Country Link
JP (1) JPS56140961A (en)

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