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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30305생성일: 2026년 10월 24일

(R)-4-Benzyl-2-oxazolidinone → 3-(2-(R)-cyclopropylmethyl-5-(3,5-difluorophenyl)-3 (S)-hydroxyl-1-oxopentyl)amino-1-methyl-5-(pyridin-2-yl)-2,3-dihydro-1H-1,4-benzodiazepin-2-one

https://huagongshe.com/ko/reaction/30305

반응식

참여 물질

역할이름HCID투입량
반응물(R)-4-Benzyl-2-oxazolidinoneHCID 2734969—
반응물3-(3,5-Difluorophenyl)propionic acidHCID 3669498—
반응물trans-3,5-Difluorocinnamic acidHCID 5374941—
반응물3-(3,5-Difluorophenyl)propanalHCID 16092530—
반응물3-(2 (R)-cyclopentylmethyl-3(S)-hydroxyl-5-phenyl-1-oxopentyl)-4(R)-(phenylmethyl)-2-oxazolidinoneHCID 18346770—
반응물2(R)-cyclopropylmethyl-5-(3,5-difluorophenyl)-3-(S)-hydroxypentanoic acid (2-oxo-1-(3-phenoxybenzyl)azapan-3-(S)-yl)amideHCID 67550039—
생성물3-(2-(R)-cyclopropylmethyl-5-(3,5-difluorophenyl)-3 (S)-hydroxyl-1-oxopentyl)amino-1-methyl-5-(pyridin-2-yl)-2,3-dihydro-1H-1,4-benzodiazepin-2-oneHCID 9807077—

반응 단계

The 3-(3,5-difluorophenyl)propanal used in the aldol reaction was prepared from trans-3,5-difluorocinnamic acid by: (1) hydrogenation to 3-(3,5-difluorophenyl)propionic acid (L. Kruse et al J. Med. Chem. 1987, 30, 486-494); (2) formation of Weinreb amide (M. Braun Synthesis 1989, 856); and (3) reduction to aldehyde (D. A. Evans J. Org. Chem. 1993, 58, 2446-2453).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423033B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-767ee72b508949e0b1fe683c50924b03
출처 메모uspto-grants-2008_09