JPS54135797A - Tetrahydro-beta-carboline derivative - Google Patents

Tetrahydro-beta-carboline derivative

Info

Publication number
JPS54135797A
JPS54135797A JP4332978A JP4332978A JPS54135797A JP S54135797 A JPS54135797 A JP S54135797A JP 4332978 A JP4332978 A JP 4332978A JP 4332978 A JP4332978 A JP 4332978A JP S54135797 A JPS54135797 A JP S54135797A
Authority
JP
Japan
Prior art keywords
tetrahydro
methyl
carboline
ethyl
formula
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
JP4332978A
Other languages
Japanese (ja)
Inventor
Toshio Wakabayashi
Kenzo 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.)
Teijin Ltd
Original Assignee
Teijin 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 Teijin Ltd filed Critical Teijin Ltd
Priority to JP4332978A priority Critical patent/JPS54135797A/en
Publication of JPS54135797A publication Critical patent/JPS54135797A/en
Pending legal-status Critical Current

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  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

NEW MATERIAL:Optically active or inactive tetrahydro-β-carboline derivative of formula I [R1 is monofunctional substitution group; m is 0, 1, 2; when m is 0, (R1)m- is H, and when m is 2, two R1s may together from a ring; R2 is H, methyl, ethyl; R3 is methyl, ethyl, propyl, butyl; C atom having × mark is asymmetric carbon).
EXAMPLE: d-3-Methoxycarbonylmethyl-9-methyl-1-oxo-1, 2, 3, 4-tetrahydro-β-carboline.
USE: Medicine having antiphlogistic, antithrombotic, analgesic, hypotensive, and psychotropic activities. Intermediate of medicines.
PROCESS: The compound I is prepared by heating an optically active or inactive ester of formula II in an alcohol such as methanol, at 50W110°C for 1W4 hours introducing HCl gas to the reaction mixture.
COPYRIGHT: (C)1979,JPO&Japio
JP4332978A 1978-04-14 1978-04-14 Tetrahydro-beta-carboline derivative Pending JPS54135797A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4332978A JPS54135797A (en) 1978-04-14 1978-04-14 Tetrahydro-beta-carboline derivative

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4332978A JPS54135797A (en) 1978-04-14 1978-04-14 Tetrahydro-beta-carboline derivative

Publications (1)

Publication Number Publication Date
JPS54135797A true JPS54135797A (en) 1979-10-22

Family

ID=12660780

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4332978A Pending JPS54135797A (en) 1978-04-14 1978-04-14 Tetrahydro-beta-carboline derivative

Country Status (1)

Country Link
JP (1) JPS54135797A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103804377A (en) * 2012-11-08 2014-05-21 复旦大学 Corynantheine compound and preparation method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103804377A (en) * 2012-11-08 2014-05-21 复旦大学 Corynantheine compound and preparation method thereof

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