JPS5629579A - Preparation of novel cyclic urethane compound - Google Patents

Preparation of novel cyclic urethane compound

Info

Publication number
JPS5629579A
JPS5629579A JP10524979A JP10524979A JPS5629579A JP S5629579 A JPS5629579 A JP S5629579A JP 10524979 A JP10524979 A JP 10524979A JP 10524979 A JP10524979 A JP 10524979A JP S5629579 A JPS5629579 A JP S5629579A
Authority
JP
Japan
Prior art keywords
formula
preparation
urethane compound
novel cyclic
compound
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
JP10524979A
Other languages
Japanese (ja)
Inventor
Dotaro Fujimoto
Toshimitsu Shigeari
Giichi Funatsukuri
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.)
Fujimoto Pharmaceutical Corp
Original Assignee
Fujimoto Pharmaceutical Corp
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 Fujimoto Pharmaceutical Corp filed Critical Fujimoto Pharmaceutical Corp
Priority to JP10524979A priority Critical patent/JPS5629579A/en
Publication of JPS5629579A publication Critical patent/JPS5629579A/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)

Abstract

NEW MATERIAL:3-Isopropyl-5-chloromethyl-2-oxazolidinone of formula I.
USE: An intermediate for the synthesis of a compound having a medicinal effect.
PROCESS: 5-Chloromethyl-2-oxazolidinone of formula II is reacted with an isopropyl halogenide of formula III (X is Br or I) in the presence of a basic catalyst, e.g. sodium or potassium hydride, in a polar reaction solvent, e.g. dehydrated dimethylformamide or dioxane, at room temperature W150°C for 1W5hr to give the compound of formula I.
COPYRIGHT: (C)1981,JPO&Japio
JP10524979A 1979-08-17 1979-08-17 Preparation of novel cyclic urethane compound Pending JPS5629579A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10524979A JPS5629579A (en) 1979-08-17 1979-08-17 Preparation of novel cyclic urethane compound

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10524979A JPS5629579A (en) 1979-08-17 1979-08-17 Preparation of novel cyclic urethane compound

Publications (1)

Publication Number Publication Date
JPS5629579A true JPS5629579A (en) 1981-03-24

Family

ID=14402371

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10524979A Pending JPS5629579A (en) 1979-08-17 1979-08-17 Preparation of novel cyclic urethane compound

Country Status (1)

Country Link
JP (1) JPS5629579A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5162354A (en) * 1991-12-20 1992-11-10 Buckman Laboratories International, Inc. 3-halo-5-halomethyl-2-oxazolidinones and their use as microbicides

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5162354A (en) * 1991-12-20 1992-11-10 Buckman Laboratories International, Inc. 3-halo-5-halomethyl-2-oxazolidinones and their use as microbicides

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