JPS54100371A - Novel imidazole c-nucleoside derivative - Google Patents

Novel imidazole c-nucleoside derivative

Info

Publication number
JPS54100371A
JPS54100371A JP776178A JP776178A JPS54100371A JP S54100371 A JPS54100371 A JP S54100371A JP 776178 A JP776178 A JP 776178A JP 776178 A JP776178 A JP 776178A JP S54100371 A JPS54100371 A JP S54100371A
Authority
JP
Japan
Prior art keywords
formula
compound
lower alkanoyl
aroyl
nucleoside derivative
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
JP776178A
Other languages
Japanese (ja)
Inventor
Toshio Atami
Yuzo Tarumi
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 JP776178A priority Critical patent/JPS54100371A/en
Publication of JPS54100371A publication Critical patent/JPS54100371A/en
Pending legal-status Critical Current

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  • Plural Heterocyclic Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

NEW MATERIAL:Imidazole C-nucleoside derivatives of formula I (R is H, lower alkanoyl, aroyl).
EXAMPLE: 2-(2',3',5'-tri-O-acetyl-β-D-ribofuranosyl)-5-hydroxyimidazole-4-carbo- xamide.
USE: Medicines used for metabolic antagonist having carcinostatic and antiviral activities.
PREPARATION: The reaction between an imide ester of formula II (A is lower alkoxy, benzylthio), its salt, preferably hydrochloride, or an ortho ester of formula III(B is lower alkyl) and aminomalon amide is conducted in an organic solvent as methanol or tetrahydrofuran at 0 - 100°C, when necessary, if R is lower alkanoyl or aroyl, the deacylation is effected, to produce the objective compound of formula I. The compound of formula II is obtained from a compound of formula IV (R' is lower alkanoyl).
COPYRIGHT: (C)1979,JPO&Japio
JP776178A 1978-01-25 1978-01-25 Novel imidazole c-nucleoside derivative Pending JPS54100371A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP776178A JPS54100371A (en) 1978-01-25 1978-01-25 Novel imidazole c-nucleoside derivative

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP776178A JPS54100371A (en) 1978-01-25 1978-01-25 Novel imidazole c-nucleoside derivative

Publications (1)

Publication Number Publication Date
JPS54100371A true JPS54100371A (en) 1979-08-08

Family

ID=11674663

Family Applications (1)

Application Number Title Priority Date Filing Date
JP776178A Pending JPS54100371A (en) 1978-01-25 1978-01-25 Novel imidazole c-nucleoside derivative

Country Status (1)

Country Link
JP (1) JPS54100371A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4728729A (en) * 1984-03-14 1988-03-01 Sumitomo Pharmaceuticals Co., Ltd. Cyanoimidazole nucleoside derivatives

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4728729A (en) * 1984-03-14 1988-03-01 Sumitomo Pharmaceuticals Co., Ltd. Cyanoimidazole nucleoside derivatives

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