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HRID 249057作成日:2026年10月25日

Ammonia → 2-amino-6-chloro-9-(beta-D-xylofuranosyl)purine

https://huagongshe.com/reaction/249057

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物N-(6-chloro-7H-purin-2-yl)acetamideHCID 6098997—
反応物2,3,5-tri-O-acetyl-beta-D-ribofuranosylpurineHCID 69884339—
触媒Mercurous ChlorideHCID 24182—
生成物2-amino-6-chloro-9-(beta-D-xylofuranosyl)purineHCID 14284102—

反応手順

The chloromercury derivative of 2-acetamido-6-chloropurine is condensed with 2,3,5-tri-O-acetyl-β-D-ribofuranosylpurine utilizing the method of Lee et. al. (1971), J. Med. Chem., 14:819. The condensation product was treated with ammonia to yield 2-amino-6-chloro-9-(β-D-xylofuranosyl)purine. Further treatment with sodium hydroxyethylmercaptide gives the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05212295
出典データセットuspto-grants-1993_05
ORD IDord-c337ce6791bb4561b9d6b1749ed0dbdb
出典メモuspto-grants-1993_05