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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41159생성일: 2026년 10월 25일

Triethylamine → (1S,2S,4R)-2-methoxy-4-(5-oxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)cyclopentyl nitrate

https://huagongshe.com/reaction/41159

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Semicarbazide hydrochlorideHCID 11236—
반응물Sodium HydroxideHCID 14798—
반응물Bis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
반응물(1S,2S,4R)-4-carbamoyl-2-methoxycyclopentyl nitrateHCID 58443610—
용매DichloromethaneHCID 6344—
생성물(1S,2S,4R)-2-methoxy-4-(5-oxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)cyclopentyl nitrateHCID 136164176—

반응 단계

(1S,2S,4R)-4-carbamoyl-2-methoxycyclopentyl nitrate (example 14, 0.14 g, 0.68 mmol) and bis(2-oxo-3-oxazolidinyl)phosphinic chloride (0.19 g, 0.75 mmol) were stirred for 10 minutes in dichloromethane (5 mL) and triethylamine (0.29 mL, 2.1 mmol). Semicarbazide hydrochloride (0.082 g, 0.73 mmol) was added and stirred at room temperature for 4 days. The solution was concentrated in vacuo and brought up in 1 M sodium hydroxide (3 mL, 3.0 mmol) to reflux for 8 hours. Purification of the crude product by reversed-phase mass-directed high-performance liquid chromatography afforded the title compound as a colorless liquid. 1H NMR (500 MHz, CDCl3) δ 1.93-1.98 (m, 1H), 2.34 (dd, J=4.1, 8.3 Hz, 2H), 2.40-2.47 (m, 1H), 2.40-2.47 (m, 1H), 3.42 (quintet, J=6.2 Hz, 1H), 3.50 (s, 3H), 3.93-3.96 (m, 1H), 5.40-5.43 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530521B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-22e3c288424f496b8bb664fc6edef27d
출처 메모uspto-grants-2013_09