JPS55167281A - Preparation of piperazine derivative or its salt - Google Patents

Preparation of piperazine derivative or its salt

Info

Publication number
JPS55167281A
JPS55167281A JP7423879A JP7423879A JPS55167281A JP S55167281 A JPS55167281 A JP S55167281A JP 7423879 A JP7423879 A JP 7423879A JP 7423879 A JP7423879 A JP 7423879A JP S55167281 A JPS55167281 A JP S55167281A
Authority
JP
Japan
Prior art keywords
salt
compound
formula
piperazine derivative
benzthiazolinone
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
JP7423879A
Other languages
Japanese (ja)
Inventor
Ikuo Ueda
Takao Watanabe
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.)
Fujisawa Pharmaceutical Co Ltd
Original Assignee
Fujisawa 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 Fujisawa Pharmaceutical Co Ltd filed Critical Fujisawa Pharmaceutical Co Ltd
Priority to JP7423879A priority Critical patent/JPS55167281A/en
Publication of JPS55167281A publication Critical patent/JPS55167281A/en
Pending legal-status Critical Current

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  • Thiazole And Isothizaole Compounds (AREA)

Abstract

PURPOSE: To obtain the titled compound, useful as a medicine, and having an anti- inflammatory action, by reducing a specific compound prepared through the reaction of a haloacetic acid with 3-(1-piperazinyl)carbonyl lower alkyl-2-benzthiazolinone.
CONSTITUTION: A compound of formula I (X is H or halogen; A is lower alkylene group; R is a carboxy group which may be protected) or its salt is reduced with an alkali metal borohydride, e.g. sodium borohydride, in a solvent, e.g. methanol or acetone, at room temperature or under cooling or heating to give a piperazine derivative of formula II or its salt. The compound of formula I can be prepared by reacting a haloacetic acid with 3-(1-piperazinyl)carbonyl lower alkyl-2-benzthiazolinone or its salt.
COPYRIGHT: (C)1980,JPO&Japio
JP7423879A 1979-06-12 1979-06-12 Preparation of piperazine derivative or its salt Pending JPS55167281A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7423879A JPS55167281A (en) 1979-06-12 1979-06-12 Preparation of piperazine derivative or its salt

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7423879A JPS55167281A (en) 1979-06-12 1979-06-12 Preparation of piperazine derivative or its salt

Publications (1)

Publication Number Publication Date
JPS55167281A true JPS55167281A (en) 1980-12-26

Family

ID=13541372

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7423879A Pending JPS55167281A (en) 1979-06-12 1979-06-12 Preparation of piperazine derivative or its salt

Country Status (1)

Country Link
JP (1) JPS55167281A (en)

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