JPS5645487A - Antirheumatic - Google Patents

Antirheumatic

Info

Publication number
JPS5645487A
JPS5645487A JP12235779A JP12235779A JPS5645487A JP S5645487 A JPS5645487 A JP S5645487A JP 12235779 A JP12235779 A JP 12235779A JP 12235779 A JP12235779 A JP 12235779A JP S5645487 A JPS5645487 A JP S5645487A
Authority
JP
Japan
Prior art keywords
formula
compound
gold
auro
antirheumatic
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.)
Granted
Application number
JP12235779A
Other languages
Japanese (ja)
Other versions
JPS6147840B2 (en
Inventor
Tadashi Iso
Masayuki Ooya
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.)
Santen Pharmaceutical Co Ltd
Original Assignee
Santen 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 Santen Pharmaceutical Co Ltd filed Critical Santen Pharmaceutical Co Ltd
Priority to JP12235779A priority Critical patent/JPS5645487A/en
Publication of JPS5645487A publication Critical patent/JPS5645487A/en
Publication of JPS6147840B2 publication Critical patent/JPS6147840B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

NEW MATERIAL:S-Auro-N-( 2-aurothio-2-methylpropanoyl )-L-cisteine of formula I and its salts.
USE: Antirheumatic.
PREPARATION: For example, the reaction of a compound of formula II (X is halogen; R is benzoyl, acetyl) with S-auro-L-cysteine gives a compound of formula III, which is treated with an alkali such as sodium hydroxide or ammonia to form a compound of formula IV. Further, the product is made to react with a monovalent gold such as gold cyanide or with a trivalent gold such as a chloroaurate in the presence of a reducing agent to produce the compound of formula I.
COPYRIGHT: (C)1981,JPO&Japio
JP12235779A 1979-09-22 1979-09-22 Antirheumatic Granted JPS5645487A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12235779A JPS5645487A (en) 1979-09-22 1979-09-22 Antirheumatic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12235779A JPS5645487A (en) 1979-09-22 1979-09-22 Antirheumatic

Publications (2)

Publication Number Publication Date
JPS5645487A true JPS5645487A (en) 1981-04-25
JPS6147840B2 JPS6147840B2 (en) 1986-10-21

Family

ID=14833894

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12235779A Granted JPS5645487A (en) 1979-09-22 1979-09-22 Antirheumatic

Country Status (1)

Country Link
JP (1) JPS5645487A (en)

Also Published As

Publication number Publication date
JPS6147840B2 (en) 1986-10-21

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