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HRID 326532作成日:2026年10月26日

Acetic acid (2R,3R,4R,5R)-3,4-diacetoxy-5-(6-chloro-2-iodo-purin-9-YL)-tetrahydro-furan-2-ylmethyl ester → 2-Iodoadenosine

https://huagongshe.com/reaction/326532

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic acid (2R,3R,4R,5R)-3,4-diacetoxy-5-(6-chloro-2-iodo-purin-9-YL)-tetrahydro-furan-2-ylmethyl esterHCID 482588—
反応物Ammonia methanolHCID 21705897—
生成物2-IodoadenosineHCID 16966290%

反応手順

6.0 g of 6-chloro-2-iodo-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)purine was added to 60 ml of methanol/ammonia (saturated at 0° C.) to cause reaction at a temperature of 60° C. for 17 hours in a sealed tube. The reaction solution was cooled, then degassed, and concentrated under reduced pressure. Crystallization of the residue from water afforded 3.94 g of 2-iodoadenosine (90% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05270304
出典データセットuspto-grants-1993_12
ORD IDord-ee01eded22734121b23cb3a8d04cef6f
出典メモuspto-grants-1993_12