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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1803972생성일: 2026년 10월 27일

(R)-4-Methyloxazolidin-2-one → (R)-3-{6-[4-(4-chlorobenzoyl)piperidine-1-carbonyl]pyridin-3-yl}-4-methyloxazolidin-2-one

https://huagongshe.com/reaction/1803972

반응식

참여 물질

역할이름HCID투입량
반응물(R)-4-Methyloxazolidin-2-oneHCID 2734858—
반응물(5-Bromopyridin-2-yl)[4-(4-chlorobenzoyl)piperidin-1-yl]methanoneHCID 58484577—
생성물(R)-3-{6-[4-(4-chlorobenzoyl)piperidine-1-carbonyl]pyridin-3-yl}-4-methyloxazolidin-2-oneHCID 5475511983.4%

반응 단계

By reaction and treatment in the same manner as in Preparation Example 31 and using (5-bromopyridin-2-yl)[4-(4-chlorobenzoyl)piperidin-1-yl]methanone (2.4 g) described in Preparation Example 35 and (R)-4-methyloxazolidin-2-one (728 mg) described in Preparation Example 25, the title compound (2.1 g) was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08354401B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-5dc47467ef784151ab188b492d73ec0b
출처 메모uspto-grants-2013_01