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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 379869생성일: 2026년 10월 25일

(1S)-2-Chloro-1-methyl-2-oxoethyl acetate → 3-[(S)-2-acetoxypropionylamino]-6-chloro-2-(4-chloropyridine-2-carbonyl)indole

https://huagongshe.com/reaction/379869

반응식

참여 물질

역할이름HCID투입량
반응물(1S)-2-Chloro-1-methyl-2-oxoethyl acetateHCID 11094804—
반응물3-Amino-6-chloro-2-(4-chloropyridine-2-carbonyl)indoleHCID 18368126—
생성물3-[(S)-2-acetoxypropionylamino]-6-chloro-2-(4-chloropyridine-2-carbonyl)indoleHCID 54371095—

반응 단계

The title compound was prepared according to the procedure described in Example 19 employing 3-amino-6-chloro-2-(4-chloropyridine-2-carbonyl)indole (Exampe 68) and (S)-(−)-2-acetoxypropionyl chloride. m.p.: 236-238° C. (recrystallized from ethyl acetate) IR(KBr)ν: 3287, 1738, 1693, 1624, 1585, 1570, 1545, 1489, 1236, 1188, 739 cm−1. 1H-NMR (DMSO-d6) δ: 12.09 (1 H, br s), 10.67 (1 H, br s), 8.77 (1 H, dd, J=5.5 and 1.8 Hz), 8.10 (1 H, t, J=1.9 Hz), 7.93 (1 H, dd, J=9.1, 1.8 Hz), 7.88 (1 H, dt, J=5.4, 2.3 Hz), 7.64 (1 H, t, J=1.9 Hz), 7.12 (1 H, dt, J=9.1, 2.1 Hz), 5.13 (1 H, q, J=6.8 Hz), 2.18 (3 H, s), 1.35 (3 H, d, J=6.9 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06300363B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-4d7a96f57d8a405292f6614f1def847a
출처 메모uspto-grants-2001_10