JPS5724362A - Preparation of pindolol - Google Patents

Preparation of pindolol

Info

Publication number
JPS5724362A
JPS5724362A JP9845980A JP9845980A JPS5724362A JP S5724362 A JPS5724362 A JP S5724362A JP 9845980 A JP9845980 A JP 9845980A JP 9845980 A JP9845980 A JP 9845980A JP S5724362 A JPS5724362 A JP S5724362A
Authority
JP
Japan
Prior art keywords
formula
indolyloxy
compound
compound shown
lactisopropylamide
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
JP9845980A
Other languages
Japanese (ja)
Inventor
Hiroshige Inoue
Kenichi Fukushima
Masanori Morita
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.)
Yamamoto Chemical Industrial Co Ltd
Original Assignee
Yamamoto Chemical Industrial 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 Yamamoto Chemical Industrial Co Ltd filed Critical Yamamoto Chemical Industrial Co Ltd
Priority to JP9845980A priority Critical patent/JPS5724362A/en
Publication of JPS5724362A publication Critical patent/JPS5724362A/en
Pending legal-status Critical Current

Links

Landscapes

  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Indole Compounds (AREA)

Abstract

PURPOSE: To obtain the titled compound useful as a β-sympatholytic agent in high purity and in high yield, by reducing β-(4-indolyloxy)lactisopropylamide as a raw material by a short process and simple operations.
CONSTITUTION: β-(4-Indolyloxy)lactisopropylamide shown by the formula I as a raw material is reduced in the presence of a reducing catalyst, e.g., aluminum borohydride, sodium boron hydride, etc. in an inert solvent, e.g., tetrahydrofuran, etc. at 0W50°C, preferably at 10W30°C, to give a compound shown by the formula II. The compound shown by the formula I is a novel compound, which is obtained by reacting a compound shown by the formula III with a compound shown by the formula IV to give novel β-(4-indolyloxy)lactic acid shown by the formula V, which is easily reacted with isopropylamine.
COPYRIGHT: (C)1982,JPO&Japio
JP9845980A 1980-07-17 1980-07-17 Preparation of pindolol Pending JPS5724362A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9845980A JPS5724362A (en) 1980-07-17 1980-07-17 Preparation of pindolol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9845980A JPS5724362A (en) 1980-07-17 1980-07-17 Preparation of pindolol

Publications (1)

Publication Number Publication Date
JPS5724362A true JPS5724362A (en) 1982-02-08

Family

ID=14220279

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9845980A Pending JPS5724362A (en) 1980-07-17 1980-07-17 Preparation of pindolol

Country Status (1)

Country Link
JP (1) JPS5724362A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9346744B2 (en) * 2014-08-28 2016-05-24 Davuluri Ramamohan Rao Process for the preparation of lacosamide and its novel intermediate

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9346744B2 (en) * 2014-08-28 2016-05-24 Davuluri Ramamohan Rao Process for the preparation of lacosamide and its novel intermediate

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