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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41161생성일: 2026년 10월 25일

Triethylamine → N-{[(1R,3S,4S)-3-methoxy-4-(nitrooxy)cyclopentyl]carbonyl}-L-valine

https://huagongshe.com/reaction/41161

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methyl valinate hydrochlorideHCID 111190—
반응물PyBOPHCID 2724699—
반응물(1R,3S,4S)-3-methoxy-4-(nitrooxy)cyclopentanecarboxylic acidHCID 58443614—
용매DichloromethaneHCID 6344—
생성물N-{[(1R,3S,4S)-3-methoxy-4-(nitrooxy)cyclopentyl]carbonyl}-L-valineHCID 4622021190.4%

반응 단계

To a solution of L-valine methyl ester hydrochloride (633 mg, 3.78 mmol), (1R,3S,4S)-3-methoxy-4-(nitrooxy)cyclopentanecarboxylic acid (755 mg, 3.78 mmol), and triethylamine (1.05 mL, 7.55 mmol) in dichloromethane (30 mL) was added PyBOP (2.95 g, 5.67 mmol). After stirring at rt overnight, the mixture was washed saturated NaHCO3 (3×50 mL) and brine (50 mL), dried over MgSO4, and concentrated. The residue was purified by flash chromatography (RediSepRf 80 g) using 0-40% EtOAc/hexane gradient, affording the title compound (1.04 g, yield 86%): 1H NMR (500 MHz, CDCl3) δ 6.50 (d, J=8.6, 1H), 5.40 (d, J=6.0, 1H), 4.55 (dd, J=4.7, 8.8, 1H), 3.92 (m, 1H), 3.77 (s, 3H), 3.47 (s, 3H), 2.96-2.91 (m, 1H), 2.52-2.46 (m, 1H), 2.38-2.32 (m, 1H), 2.24-2.17 (m, 2H), 2.07-2.01 (m, 1H), 0.97 (d, J=6.9, 3H), 0.92 (d, J=6.9, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530521B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-90c8cd4faad3491fadd63ecbcc30f34c
출처 메모uspto-grants-2013_09