JPS5681581A - Preparation of antispasmodic agent - Google Patents

Preparation of antispasmodic agent

Info

Publication number
JPS5681581A
JPS5681581A JP15813279A JP15813279A JPS5681581A JP S5681581 A JPS5681581 A JP S5681581A JP 15813279 A JP15813279 A JP 15813279A JP 15813279 A JP15813279 A JP 15813279A JP S5681581 A JPS5681581 A JP S5681581A
Authority
JP
Japan
Prior art keywords
compound
formula
reacted
piperidine
reacting
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.)
Granted
Application number
JP15813279A
Other languages
Japanese (ja)
Other versions
JPS638945B2 (en
Inventor
Kazuo Kikazawa
Mineji Hiiragi
Haruhide Ishimaru
Toshihisa Nakamura
Keiko Shiroyama
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.)
Aska Pharmaceutical Co Ltd
Original Assignee
Grelan 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 Grelan Pharmaceutical Co Ltd filed Critical Grelan Pharmaceutical Co Ltd
Priority to JP15813279A priority Critical patent/JPS5681581A/en
Publication of JPS5681581A publication Critical patent/JPS5681581A/en
Publication of JPS638945B2 publication Critical patent/JPS638945B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE: To obtain the titled substance having an antiacetylcholinergic action readily, by reacting a 2-cychlohexyl-γ-2-phenyl-t-4-halogenomethyl-1,3-dioxolane as an intermediate with piperidine.
CONSTITUTION: A compound of formula I (X is halogen) is reacted with piperidine to give a compound of formula II, which is then reacted with a methyl halide to form a quaternary ammonium salt or the compound of formula I is reacted with N- methylpiperidine to afford the compound of formula III. The compound of formula I is obtained by reacting a compound of formula IV with an inorganic halide in high yield, and the isomer cannot be easily separated by the conventional method. The compound of formula III which is a pure trans isomer can be obtained from the compound of formula I and is useful for preparing the trans isomer of the compound of formula V useful as a ganglion blocking agent.
COPYRIGHT: (C)1981,JPO&Japio
JP15813279A 1979-12-07 1979-12-07 Preparation of antispasmodic agent Granted JPS5681581A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15813279A JPS5681581A (en) 1979-12-07 1979-12-07 Preparation of antispasmodic agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15813279A JPS5681581A (en) 1979-12-07 1979-12-07 Preparation of antispasmodic agent

Publications (2)

Publication Number Publication Date
JPS5681581A true JPS5681581A (en) 1981-07-03
JPS638945B2 JPS638945B2 (en) 1988-02-25

Family

ID=15664971

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15813279A Granted JPS5681581A (en) 1979-12-07 1979-12-07 Preparation of antispasmodic agent

Country Status (1)

Country Link
JP (1) JPS5681581A (en)

Also Published As

Publication number Publication date
JPS638945B2 (en) 1988-02-25

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