JPS5492989A - Preparation of substituted theobromine - Google Patents

Preparation of substituted theobromine

Info

Publication number
JPS5492989A
JPS5492989A JP15747977A JP15747977A JPS5492989A JP S5492989 A JPS5492989 A JP S5492989A JP 15747977 A JP15747977 A JP 15747977A JP 15747977 A JP15747977 A JP 15747977A JP S5492989 A JPS5492989 A JP S5492989A
Authority
JP
Japan
Prior art keywords
theobromine
formula
give
derivative
substituted
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
JP15747977A
Other languages
Japanese (ja)
Inventor
Hirokiyo Ichinomiya
Yukinari Kobayashi
Takanori Sone
Mikio Wakabayashi
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.)
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry 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 Asahi Chemical Industry Co Ltd filed Critical Asahi Chemical Industry Co Ltd
Priority to JP15747977A priority Critical patent/JPS5492989A/en
Publication of JPS5492989A publication Critical patent/JPS5492989A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE: To obtain a substituted theobromine which is a vasolidator and a hematocytolysis enhancer of low toxicity in a high yield with ease, by reacting a theobromine derivative with an acetoacetic ester in the presence of a base, followed by hydrolysis and decarboxylation.
CONSTITUTION: A theobromine derivative of formula I is reacted with a compound of formula II: (R is lower alkyl group) in the presence of an alkali metal alkoxide, or hydride in a solvent, e.g. methanol or DMF, preferably at 60W120°C to give a reaction product, which is then hydrolyzed by NaOH, etc., and decarboxylated by sulfuric acid under refluxing and heating, to give 1-(5-oxohexyl)theobromine of formula III.
EFFECT: The raw material is easily available, and the objective compound can be readily purified with little formation of by-products.
COPYRIGHT: (C)1979,JPO&Japio
JP15747977A 1977-12-28 1977-12-28 Preparation of substituted theobromine Pending JPS5492989A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15747977A JPS5492989A (en) 1977-12-28 1977-12-28 Preparation of substituted theobromine

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15747977A JPS5492989A (en) 1977-12-28 1977-12-28 Preparation of substituted theobromine

Publications (1)

Publication Number Publication Date
JPS5492989A true JPS5492989A (en) 1979-07-23

Family

ID=15650568

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15747977A Pending JPS5492989A (en) 1977-12-28 1977-12-28 Preparation of substituted theobromine

Country Status (1)

Country Link
JP (1) JPS5492989A (en)

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