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HRID 48559作成日:2026年10月25日

Dimethylformamide → (R)-9-[2-(N-Boc-L-valyloxymethyl)4-(stearoyloxy)butyl]guanine

https://huagongshe.com/reaction/48559

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物Boc-L-ValineHCID 83693—
反応物(R)-9-[2-Hydroxymethyl-4-(stearoyloxy)butyl]guanineHCID 136343267—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物(R)-9-[2-(N-Boc-L-valyloxymethyl)4-(stearoyloxy)butyl]guanineHCID 13582946039.3%

反応手順

A mixture of N-Boc-L-valine (528 mg; 2.1 mmol) and N,N′-dicyclohexyl carbodiimide (250 mg; 1.21 mg) in dichloromethane (20 ml) was stirred over night at room temperature, dicyclohexylurea filtered off and extracted with a small volume of dichloromethane, and the filtrate evaporated in vacuo to a small volume. (R)-9-[2-Hydroxymethyl-4-(stearoyloxy)butyl]guanine (340 mg; 0.654 mmol), 4-dimethylaminopyridine (25 mg; 0.205 mmol), and dry N,N-dimethylformamide (15 ml) were added and the mixture was stirred for 4 h at 50° C. under N2. The solvent was evaporated in vacuo to a small volume. Column chromatography on silica gel, then on aluminum oxide (ethyl acetate:methanol: water 15:2:1 as eluent) gave 185 mg (39%) pure title compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06703394B2
出典データセットuspto-grants-2004_03
ORD IDord-fd5c64ed8b2a4ec8b5c23cabdd62366f
出典メモuspto-grants-2004_03