JPS56158743A - Novel aminoalkyl ether derivative - Google Patents

Novel aminoalkyl ether derivative

Info

Publication number
JPS56158743A
JPS56158743A JP4275181A JP4275181A JPS56158743A JP S56158743 A JPS56158743 A JP S56158743A JP 4275181 A JP4275181 A JP 4275181A JP 4275181 A JP4275181 A JP 4275181A JP S56158743 A JPS56158743 A JP S56158743A
Authority
JP
Japan
Prior art keywords
formula
aryls
compound shown
aryl
substituents
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
JP4275181A
Other languages
Japanese (ja)
Inventor
Hajime Kawakami
Keiichi Ono
Sumimoto Katsube
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical 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
Priority claimed from AU56893/80A external-priority patent/AU532700B2/en
Application filed by Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Publication of JPS56158743A publication Critical patent/JPS56158743A/en
Pending legal-status Critical Current

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  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

NEW MATERIAL:The titled compound shown by the formula I [C=W is CH-O, or C=NO; R1 and R2 are unsubstituted aryl and aryl having 1W3 substituent, e.g., halogen, etc. with the proviso that the case where both R1 and R2 are unsubstituted aryls or aryls having only 1W3 substituents, e.g., halogens, etc. is omitted; A is group shown by the formula II (R3 and R4 are H, lower alkyl, etc.); l1 and l2 are lower alkyl chain, etc.] and its salt.
EXAMPLE: 1-[ 3-(N, N-Dimethyl, amino) propoxy ]-1-( p-isopropy-1-thiophenyl )-4- phenylbutane.
USE: A remedy for cerebrovascular disorder or crown blood disorder. Having vasodilating action, spasmolytic actions, etc.
PROCESS: A compound shown by the formula III (R5 and R6 are unsubstituted aryl and aryl having 1W3 substituents, e.g., halogen, etc. with the provito that the case where both R5 and R6 are unsubstituted aryls or aryls having only 1W3 substituents, e.g., halogens, etc. is omitted) is reacted with a compound shown by the formula HA, and, if necessary, the prepared compound is nitrated, to give the titled compound shown by the formula I.
COPYRIGHT: (C)1981,JPO&Japio
JP4275181A 1980-03-27 1981-03-23 Novel aminoalkyl ether derivative Pending JPS56158743A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
AU56893/80A AU532700B2 (en) 1979-04-02 1980-03-27 Diphenylalkanoether

Publications (1)

Publication Number Publication Date
JPS56158743A true JPS56158743A (en) 1981-12-07

Family

ID=3742413

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4275181A Pending JPS56158743A (en) 1980-03-27 1981-03-23 Novel aminoalkyl ether derivative

Country Status (1)

Country Link
JP (1) JPS56158743A (en)

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