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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1893836생성일: 2026년 10월 25일

Trifluoroacetic acid → {N-[(1R)-1-Carbamoyl-3-methyl-butyl]-N-(4-chlorobenzenesulfonyl)amino}acetic acid

https://huagongshe.com/reaction/1893836

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물{N-[(1R)-1-Carbamoyl-3-methyl-butyl]-N-(4-chlorobenzenesulfonyl)amino}acetic acid tert-butyl esterHCID 59001051—
용매DichloromethaneHCID 6344—
생성물{N-[(1R)-1-Carbamoyl-3-methyl-butyl]-N-(4-chlorobenzenesulfonyl)amino}acetic acidHCID 59001083—

반응 단계

Trifluoroacetic acid (15 mL) was added to a solution of {N-[(1R)-1-carbamoyl-3-methyl-butyl]-N-(4-chlorobenzenesulfonyl)amino}acetic acid tert-butyl ester (0.50 g, 1.2 mmol) in CH2Cl2 (15 mL). The reaction was stirred at rt for 4 h. The reaction was then concentrated to a white solid (0.40 g, 92%), which was used without further purification. MS (ESI), (M+H)+363.1; 1H NMR (DMSO-d6, 500 MHz) δ 7.90 (dd, 2H, J=2.0, 6.8), 7.65 (dd, 2H, J=2.0, 6.8), 7.60 (s, 1H), 7.06 (s, 1H), 4.32 (d, 1H, J=18), 4.12 (t, 1H, J=8.0), 4.02 (d, 1H, J=18), 1.55-1.65 (m, 1H), 1.35-1.45 (m, 2H), 0.78 (d, 3H, J=6.1), 0.73 (d, 3H, J=6.1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08513253B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-08fd2f3cb77a4b3f85a0f93b1a2df9ec
출처 메모uspto-grants-2013_08