JPS57140780A - Preparation of dibenzoxepine derivative - Google Patents

Preparation of dibenzoxepine derivative

Info

Publication number
JPS57140780A
JPS57140780A JP1121082A JP1121082A JPS57140780A JP S57140780 A JPS57140780 A JP S57140780A JP 1121082 A JP1121082 A JP 1121082A JP 1121082 A JP1121082 A JP 1121082A JP S57140780 A JPS57140780 A JP S57140780A
Authority
JP
Japan
Prior art keywords
compound
agent
formula
derivative
oxepin
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
JP1121082A
Other languages
Japanese (ja)
Inventor
Katsujiro Ueno
Hiroaki Tagawa
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.)
Daiichi Pharmaceutical Co Ltd
Original Assignee
Daiichi 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 Daiichi Pharmaceutical Co Ltd filed Critical Daiichi Pharmaceutical Co Ltd
Priority to JP1121082A priority Critical patent/JPS57140780A/en
Publication of JPS57140780A publication Critical patent/JPS57140780A/en
Pending legal-status Critical Current

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  • Pyrane Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

NEW MATERIAL:The 6,11-dihydrodibenz[b,e]oxepin-11-one derivative of formulaI(R is H, halogen or lower alkoxy; R1 is H or lower alkyl).
EXAMPLE: 6,11-Dihydro-11-oxodibenz[b,e]oxepin-2-acetic acid methyl ester.
USE: Antiphlogistic agent, analgesic and antipyretic agent, and blood platelet coagulation inhibiting agent.
PROCESS: The compound of formulaIis prepared by treating the compound of formula II with thallium trinitrate in an alcoholic solvent in the presence of an acid catalyst (e.g. perchloric acid, nitric acid, etc.), and if necessary, hydrolyzing the product. The reaction is carried out at 0W60°C for 1W20 hours. The compound of formula II is also a novel substance, and can be obtained by oxidizing the compound of formula III with an oxidizing agent (e.g. chromic anhydride).
COPYRIGHT: (C)1982,JPO&Japio
JP1121082A 1982-01-27 1982-01-27 Preparation of dibenzoxepine derivative Pending JPS57140780A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1121082A JPS57140780A (en) 1982-01-27 1982-01-27 Preparation of dibenzoxepine derivative

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1121082A JPS57140780A (en) 1982-01-27 1982-01-27 Preparation of dibenzoxepine derivative

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP10812974A Division JPS602308B2 (en) 1974-09-19 1974-09-19 Method for producing dibenzoxepine derivatives

Publications (1)

Publication Number Publication Date
JPS57140780A true JPS57140780A (en) 1982-08-31

Family

ID=11771633

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1121082A Pending JPS57140780A (en) 1982-01-27 1982-01-27 Preparation of dibenzoxepine derivative

Country Status (1)

Country Link
JP (1) JPS57140780A (en)

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