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HRID 57472作成日:2026年10月25日

Water → (R)-4-((R)-1-(tert-butoxy)ethyl)-3-(2-(((S)-1-phenylethyl)amino)pyrimidin-4-yl)oxazolidin-2-one

https://huagongshe.com/reaction/57472

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物1-Phenethylamine, (-)-HCID 75818—
反応物DiisopropylethylamineHCID 81531—
反応物(R)-4-((R)-1-(tert-butoxy)ethyl)-3-(2-fluoropyrimidin-4-yl)oxazolidin-2-oneHCID 90415866—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Ethyl AcetateHCID 8857—
溶媒HeptaneHCID 8900—
生成物(R)-4-((R)-1-(tert-butoxy)ethyl)-3-(2-(((S)-1-phenylethyl)amino)pyrimidin-4-yl)oxazolidin-2-oneHCID 9041611793%

反応手順

A solution of (R)-4-((R)-1-(tert-butoxy)ethyl)-3-(2-fluoropyrimidin-4-yl)oxazolidin-2-one (112 mg, 0.40 mmol), (S)-1-phenylethanamine (58 mg, 0.48 mmol, 1.2 equiv), and DIPEA (153 mg, 1.2 mmol, 3.0 equiv) in DMSO (4.0 mL) was heated at 100° C. for 90 min. The reaction mixture was poured into 5 ml of water, extracted with EA (2×10 ml), the solvent was removed to yield the crude product. Silica gel column chromatography (ethyl acetate in heptane 10 to 50%) provided the pure product (142 mg, white solid) in a 93% yield. HRMS m/z 385.2231 (M+H)+, RT=3.35 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434719B2
出典データセットuspto-grants-2016_09
ORD IDord-b06878a155664fa0b46e4ee53ebfd747
出典メモuspto-grants-2016_09