JPS57140777A - Preparation of piperazine derivative - Google Patents

Preparation of piperazine derivative

Info

Publication number
JPS57140777A
JPS57140777A JP56116542A JP11654281A JPS57140777A JP S57140777 A JPS57140777 A JP S57140777A JP 56116542 A JP56116542 A JP 56116542A JP 11654281 A JP11654281 A JP 11654281A JP S57140777 A JPS57140777 A JP S57140777A
Authority
JP
Japan
Prior art keywords
compound
formula
daily
preparation
action
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
JP56116542A
Other languages
Japanese (ja)
Inventor
Hiroshi Murai
Yoshiaki Aoyanagi
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.)
Nippon Shinyaku Co Ltd
Original Assignee
Nippon Shinyaku 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 Nippon Shinyaku Co Ltd filed Critical Nippon Shinyaku Co Ltd
Priority to JP56116542A priority Critical patent/JPS57140777A/en
Publication of JPS57140777A publication Critical patent/JPS57140777A/en
Pending legal-status Critical Current

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

NEW MATERIAL:The N-substituted trialkoxybenzylpiperazine derivative of formulaI(R is methyl or ethyl; Z is group of formula II; n is 2W8).
USE: It has pharmacological activities to the cornary circulation system, e.g. coronary vessel dilating action, cardiac motion suppressing action, etc., and is useful as a medicine such as remedy for ischemic cardiopathy. Dose: preferably about 10W500mg daily for oral administration and about 1W50mg daily for intravenous injection to human body.
PROCESS: The compound of formulaIcan be prepared by reacting the compound of formula III with the compound of formula IV (X is halogen) in the presence of a proper acid scavenger such as alkali metal carbonate, caustic alkali, etc. in an inert solvent such as alcohol, dioxane, etc.
COPYRIGHT: (C)1982,JPO&Japio
JP56116542A 1981-07-24 1981-07-24 Preparation of piperazine derivative Pending JPS57140777A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56116542A JPS57140777A (en) 1981-07-24 1981-07-24 Preparation of piperazine derivative

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56116542A JPS57140777A (en) 1981-07-24 1981-07-24 Preparation of piperazine derivative

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP2744377A Division JPS53112887A (en) 1976-04-09 1977-03-12 Production of n-substituted trialkoxybenzylpiperazine derivative

Publications (1)

Publication Number Publication Date
JPS57140777A true JPS57140777A (en) 1982-08-31

Family

ID=14689690

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56116542A Pending JPS57140777A (en) 1981-07-24 1981-07-24 Preparation of piperazine derivative

Country Status (1)

Country Link
JP (1) JPS57140777A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4725597A (en) * 1983-03-21 1988-02-16 Boehringer Ingelheim Ltd. Bis(piperazinyl or homopiperazinyl)alkanes

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4725597A (en) * 1983-03-21 1988-02-16 Boehringer Ingelheim Ltd. Bis(piperazinyl or homopiperazinyl)alkanes

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