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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 57472생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/57472

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1-Phenethylamine, (-)-HCID 75818—
반응물DiisopropylethylamineHCID 81531—
반응물(R)-4-((R)-1-(tert-butoxy)ethyl)-3-(2-fluoropyrimidin-4-yl)oxazolidin-2-oneHCID 90415866—
용매Dimethyl SulfoxideHCID 679—
용매Ethyl AcetateHCID 8857—
용매HeptaneHCID 8900—
생성물(R)-4-((R)-1-(tert-butoxy)ethyl)-3-(2-(((S)-1-phenylethyl)amino)pyrimidin-4-yl)oxazolidin-2-oneHCID 9041611793%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434719B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-b06878a155664fa0b46e4ee53ebfd747
출처 메모uspto-grants-2016_09