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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20177생성일: 2026년 10월 23일

Sodium hydride → Benzyl 6-[(tert-butoxycarbonyl)amino]-5-oxo-4-(2,2,2-trifluoroethyl)-1,4-diazepane-1-carboxylate

https://huagongshe.com/ko/reaction/20177

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2,2,2-Trifluoroethyl trichloromethanesulphonateHCID 90027—
반응물TrichloromethanesulfonateHCID 22293222—
반응물Benzyl 6-[(tert-butoxycarbonyl)amino]-5-oxo-1,4-diazepane-1-carboxylateHCID 22293224—
용매DimethylformamideHCID 6228—
생성물Benzyl 6-[(tert-butoxycarbonyl)amino]-5-oxo-4-(2,2,2-trifluoroethyl)-1,4-diazepane-1-carboxylateHCID 2229325642%

반응 조건

온도-35 °C

반응 단계

Sodium hydride (60% dispersion in mineral oil; 180 mg, 4.43 mmol) was added to a solution of benzyl 6-[(tert-butoxycarbonyl)amino]-5-oxo-1,4-diazepane-1-carboxylate (1.34 g, 3.69 mmol) in N,N-dimethylformamide (25 mL) at −35° C. After 15 min, 2,2,2-trifluoroethyl trichloromethanesulfonate (0.911 mL, 5.54 mmol) was added and the reaction was stirred at −35° C. After 2 h, an additional amount of sodium hydride (100 mg, 2.5 mmol) and trichloromethanesulfonate (0.500 mL, 3.04 mmol) were added. After 18 h, the reaction was quenched with water and the mixture was extracted with ethyl acetate. The organic layer was washed with water (3×), saturated brine, dried over magnesium sulfate, filtered and concentrated. Purification by silica gel chromatography (hexanes→30% ethyl acetate/hexanes) gave the title compound (690 mg). MS 446 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745427B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-74b91a26d6574e45ac7bdc8424e21ec0
출처 메모uspto-grants-2010_06