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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 83527생성일: 2026년 10월 25일

(S)-4-Benzyl-2-oxazolidinone → (S)-4-Benzyl-3-[(S)-1-(2,4-dimethoxybenzyl)-5-oxopyrrolidine-3-carbonyl]-2-oxazolidinone

https://huagongshe.com/reaction/83527

반응식

참여 물질

역할이름HCID투입량
반응물(S)-4-Benzyl-2-oxazolidinoneHCID 736225—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-(2,4-Dimethoxybenzyl)-5-oxopyrrolidine-3-carboxylic acidHCID 11254461—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매ChloroformHCID 6212—
생성물(S)-4-Benzyl-3-[(S)-1-(2,4-dimethoxybenzyl)-5-oxopyrrolidine-3-carbonyl]-2-oxazolidinoneHCID 8668036454.8%

반응 단계

To a solution of 1-(2,4-dimethoxybenzyl)-5-oxopyrrolidine-3-carboxylic acid (20 g) prepared according to the same procedures as Preparation 5 in chloroform (200 ml) were sequentially added (S)-4-benzyl-2-oxazolidinone (15.2 g) and WSC.HCl (16.4 g), 4-(dimethylamino)pyridine (4.4 g) at room temperature, and the mixture was stirred for 3 hours. This reaction solution was washed with a 5 wt % aqueous solution of sodium hydrogen carbonate and a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=1/1 to 1/3), subjected to azeotropic drying with toluene, and dried under reduced pressure to give the titled compound (17.2 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846746B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-fe9aac0101e04f9ea94e4a4d82e87b01
출처 메모uspto-grants-2014_09