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JPS604199A Expired / Lapsed JP ⏱️ 0.0 years remaining

Preparation of nucleotide

Assignee: Daiichi Pharmaceutical Co Ltd
•
Filing: 1983-06-20
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Granted: —
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Expires: 2003-06-20
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Abstract

Abstract PURPOSE:To prepare a nucleotide useful as a synthetic raw material of DNA and PNA, stably, in a short time, by reacting a nucleoside with cyclohexylammonium 0-chlorophenyl-beta-cyanoethylphosphate (a novel compound). CONSTITUTION:The nucleotide of formula III is prepared by reacting a nucleoside of formula I [B is (protected) base such as N-benzoylcytosine, N-benzoyladenine, N-isobutylylguanine, thymine, etc.; R<1> is H or OH protected with a group for protecting hydroxyl group of sugars; R<2> is sugar OH-protecting group such as dimethoxytrityl] with a phosphorylation agent comprising the novel cyclohexylammonium o-chlorophenyl-beta-cyanoethylphosphate of formula II preferably at a molar ratio of 1:1-several moles in the presence of a condensation agent at room temperature. The above novel compound can be synthesized e.g. from o-chlorophenyl phosphorodichloridate.

Inventors

  • 👤 Koji Yamada
  • 👤 晃司 山田
  • 👤 Masanobu Naruto
  • 👤 成戸 昌信
  • 👤 Renzo Domori
  • 👤 堂森 廉三

Bibliographic Details

Application Number —
Jurisdiction JP
Data Source google_patents
Last Synchronized 2026-11-04 08:41
CPC Classifications
Y; Y02; Y02P; Y02P20/00; Y02P20/50; Y02P20/55

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