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HRID 1882543作成日:2026年10月25日

Triethylamine → Acetic acid {(1S,2R,3S,4R)-4-[2-chloro-6-((S)-1-hydroxymethyl-2-phenyl-ethylamino)-purin-9-yl]-2,3-dihydroxy-cyclopentylcarbamoyl}-methyl ester

https://huagongshe.com/reaction/1882543

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物phenylalaninol, (S)-HCID 447213—
反応物Acetic acid [(1S,2R,3S,4R)-4-(2,6-dichloro-purin-9-yl)-2,3-dihydroxy-cyclopentyl-carbamoyl]-methyl esterHCID 59419014—
溶媒DichloromethaneHCID 6344—
生成物Acetic acid {(1S,2R,3S,4R)-4-[2-chloro-6-((S)-1-hydroxymethyl-2-phenyl-ethylamino)-purin-9-yl]-2,3-dihydroxy-cyclopentylcarbamoyl}-methyl esterHCID 86632439—

反応手順

The title compound is prepared by combining acetic acid [(1S,2R,3S,4R)-4-(2,6-dichloro-purin-9-yl)-2,3-dihydroxy-cyclopentyl-carbamoyl]-methyl ester (1 equivalent) and (S)-2-amino-3-phenyl-propan-1-ol 1 equivalent) in dichloromethane with triethylamine (1.1 equivalents) and stirring overnight. The reaction is diluted with dichloromethane, and washed consecutively with 0.1M hydrochloric acid, water and brine, before drying over magnesium sulfate. Filtration and removal of the volatile components under reduced pressure, affords the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08318750B2
出典データセットuspto-grants-2012_11
ORD IDord-ee01ee5123264b1082b41915788727d2
出典メモuspto-grants-2012_11