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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 2,2,2-Trifluoroethyl trichloromethanesulphonate | HCID 90027 | — |
| 반응물 | Trichloromethanesulfonate | HCID 22293222 | — |
| 반응물 | Benzyl 6-[(tert-butoxycarbonyl)amino]-5-oxo-1,4-diazepane-1-carboxylate | HCID 22293224 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Benzyl 6-[(tert-butoxycarbonyl)amino]-5-oxo-4-(2,2,2-trifluoroethyl)-1,4-diazepane-1-carboxylate | HCID 22293256 | 42% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07745427B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-74b91a26d6574e45ac7bdc8424e21ec0 |
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| 출처 메모 | uspto-grants-2010_06 |
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