SU134267A1 - The method of obtaining hypoxanthine (alpha-oxypurine) - Google Patents

The method of obtaining hypoxanthine (alpha-oxypurine)

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Publication number
SU134267A1
SU134267A1 SU658161A SU658161A SU134267A1 SU 134267 A1 SU134267 A1 SU 134267A1 SU 658161 A SU658161 A SU 658161A SU 658161 A SU658161 A SU 658161A SU 134267 A1 SU134267 A1 SU 134267A1
Authority
SU
USSR - Soviet Union
Prior art keywords
hypoxanthine
oxypurine
alpha
obtaining
cyanacetamide
Prior art date
Application number
SU658161A
Other languages
Russian (ru)
Inventor
Р.Г. Глушков
О.Ю. Магидсон
Original Assignee
Р.Г. Глушков
О.Ю. Магидсон
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 Р.Г. Глушков, О.Ю. Магидсон filed Critical Р.Г. Глушков
Priority to SU658161A priority Critical patent/SU134267A1/en
Application granted granted Critical
Publication of SU134267A1 publication Critical patent/SU134267A1/en

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Description

T-LN-соT-LN-co

2bK-.ONH,-I У}|+ +  2bK-.ONH, -I Y} | + +

Исходный нродукг представл ет собой доступное соединение, получающеес  при нитрозировании цианапетамида и последующего восстановлени  изонитрозоцианацетамида.The starting material is an available compound resulting from the nitrosation of cyanaptamide and the subsequent reduction of isonitroso cyanacetamide.

Эгот способ имеет меньшее число стадий по сравнению со способом Шоу и прост в осу 1ествлении.This method has a smaller number of stages in comparison with the Shaw method and is easy to use.

П р и м е р. K 6 г технического аминоцианацетамида с т. пл. 120-122 добавл ют 36 Л1Л формамида, при последующем размешивании оисходит постепенное растворение осадка и разогревание массы до 27°. ПослеPRI me R. K 6 g of technical aminocyanacetamide with m. Pl. 120-122 36 L1L of formamide is added, with subsequent stirring, the precipitate gradually dissolves and the mass is heated to 27 °. After

№.134267 2самопроизвольного снижени  температуры до 22° образовавшийс  раствор кип т т при температуре 180-190 три часа, затем избыток формаад ида отгон ют в вакууме, остаток промывают водой и спиртом. Выход гипоксантина 3,9 г, не плавитс  до 360°.No.134267 2 spontaneously lowering the temperature to 22 °, the resulting solution is boiled at 180-190 for three hours, then the excess formade ida is distilled off in vacuum, the residue is washed with water and alcohol. Hypoxanthine yield 3.9 g, does not melt to 360 °.

Предмет изобретени Subject invention

Способ получени  гипоксантина (6-оксипурина), отличающийс  тем. что а-амино-а-цианацетамид нагревают с формамидом до 190.A method for producing hypoxanthine (6-hydroxypurine), characterized in that. that a-amino-a-cyanacetamide is heated with formamide to 190.

SU658161A 1960-03-09 1960-03-09 The method of obtaining hypoxanthine (alpha-oxypurine) SU134267A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU658161A SU134267A1 (en) 1960-03-09 1960-03-09 The method of obtaining hypoxanthine (alpha-oxypurine)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU658161A SU134267A1 (en) 1960-03-09 1960-03-09 The method of obtaining hypoxanthine (alpha-oxypurine)

Publications (1)

Publication Number Publication Date
SU134267A1 true SU134267A1 (en) 1960-11-30

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
SU658161A SU134267A1 (en) 1960-03-09 1960-03-09 The method of obtaining hypoxanthine (alpha-oxypurine)

Country Status (1)

Country Link
SU (1) SU134267A1 (en)

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