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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41160생성일: 2026년 10월 25일

Benzenesulfonamide → (1S,2S,4R)-2-methoxy-4-[(phenylsulfonyl)carbamoyl]cyclopentyl nitrate

https://huagongshe.com/reaction/41160

반응식

참여 물질

역할이름HCID투입량
반응물BenzenesulfonamideHCID 7370—
반응물TriethylamineHCID 8471—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물(1R,3S,4S)-3-methoxy-4-(nitrooxy)cyclopentanecarboxylic acidHCID 58443614—
용매DichloromethaneHCID 6344—
생성물(1S,2S,4R)-2-methoxy-4-[(phenylsulfonyl)carbamoyl]cyclopentyl nitrateHCID 46220316—

반응 단계

A mixture of (1R,3S,4S)-3-methoxy-4-(nitrooxy)cyclopentanecarboxylic acid (example 1, 105 mg, 0.510 mmol) and benzenesulfonamide (173 mg, 1.10 mmol) was dissolved in dichloromethane (4 mL). Triethylamine (240 pl, 1.72 mmol) was added, followed by O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (291 mg, 0.765 mmol). The reaction mixture was stirred for 12 hours. Purification of the crude product by reversed-phase mass-directed high-performance liquid chromatography afforded the title compound as a white solid. 1H NMR (500 MHz, CDCl3) δ 1.93-2.02 (m, 1H), 2.15-2.26 (m, 2 H), 2.34 (dt, J=6.8, 15.7 Hz, 1H), 2.93-3.01 (m, 1H), 3.50 (s, 3H), 3.90-3.94 (m, 1H), 5.33-5.37 (m, 1H), 7.55 (t, J=7.8 Hz, 2H), 7.65 (t,J=7.5 Hz, 1H), 8.03-8.07 (m, 2H), 9.42 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530521B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-c4090a33454e4f25bcd5db6c101fe67a
출처 메모uspto-grants-2013_09