JPS57188542A - Preparation of tetrahydronaphthacene derivative - Google Patents

Preparation of tetrahydronaphthacene derivative

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Publication number
JPS57188542A
JPS57188542A JP7394681A JP7394681A JPS57188542A JP S57188542 A JPS57188542 A JP S57188542A JP 7394681 A JP7394681 A JP 7394681A JP 7394681 A JP7394681 A JP 7394681A JP S57188542 A JPS57188542 A JP S57188542A
Authority
JP
Japan
Prior art keywords
compound
formula
reacting
tetrahydronaphthacene
hydrolyzing
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
JP7394681A
Other languages
Japanese (ja)
Inventor
Michihisa Muramatsu
Hiromi Sato
Kikuo Ishizumi
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
Application filed by Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP7394681A priority Critical patent/JPS57188542A/en
Publication of JPS57188542A publication Critical patent/JPS57188542A/en
Pending legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

PURPOSE: To prepare the titled compound useful as a drug, without protecting the side chain ketone group, by using a compound such as 9-acetyl-6,9,11-trihydroxy-7,8,9,10-tetrahydronaphthacene-5,12-dione, as a raw material.
CONSTITUTION: The objective compound of formula VII (R' is H or alkanoyl) can be prepared by (1) reacting the compound of formulaIwith a halogenation reagent such as N-bromosuccinimide to obtain the compound of formula II (X is halogen), (2) reacting the product with a carboxylic acid metal salt of formula III (R is lower in a solvent such as diethyl ether in the presence of a halogenation reagent such as chlorine to obtain the compound of formula V, (4) reacting the comound with sodium salt or potassium salt of trifluoroacetic acid and hydrolyzing the resultant compound of formula VI, and (5) if necessary further hydrolyzing the produced compound.
COPYRIGHT: (C)1982,JPO&Japio
JP7394681A 1981-05-15 1981-05-15 Preparation of tetrahydronaphthacene derivative Pending JPS57188542A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7394681A JPS57188542A (en) 1981-05-15 1981-05-15 Preparation of tetrahydronaphthacene derivative

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7394681A JPS57188542A (en) 1981-05-15 1981-05-15 Preparation of tetrahydronaphthacene derivative

Publications (1)

Publication Number Publication Date
JPS57188542A true JPS57188542A (en) 1982-11-19

Family

ID=13532769

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7394681A Pending JPS57188542A (en) 1981-05-15 1981-05-15 Preparation of tetrahydronaphthacene derivative

Country Status (1)

Country Link
JP (1) JPS57188542A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2020117468A (en) * 2019-01-25 2020-08-06 日本マイクロバイオファーマ株式会社 Production method of 14-bromo anthracycline

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2020117468A (en) * 2019-01-25 2020-08-06 日本マイクロバイオファーマ株式会社 Production method of 14-bromo anthracycline

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