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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133130생성일: 2026년 10월 26일

Sodium hydride → 1,1-Dimethylethyl N-((3R,6S)-6-(2,3-difluorophenyl)hexahydro-2-oxo-1-(2,2,2-trifluoroethyl)-1H-azepin-3-yl)carbamate

https://huagongshe.com/reaction/133130

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2,2,2-Trifluoroethyl trichloromethanesulphonateHCID 90027—
반응물tert-Butyl [(3R,6S)-6-(2,3-difluorophenyl)-2-oxoazepan-3-yl]carbamateHCID 23657400—
용매DimethylformamideHCID 6228—
생성물1,1-Dimethylethyl N-((3R,6S)-6-(2,3-difluorophenyl)hexahydro-2-oxo-1-(2,2,2-trifluoroethyl)-1H-azepin-3-yl)carbamateHCID 86595042—

반응 단계

Sodium hydride (60% dispersion in mineral oil, 70.7 mg, 1.06 mmol) was added to a solution of tert-butyl (3R,6S)-6-(2,3-difluorophenyl)-2-oxoazepan-3-ylcarbamate from Step E (301 mg, 0.884 mmol) in DMF (7 mL) at −35° C. After 15 min, 2,2,2-trifluoroethyl trichloromethanesulfonate (0.314 mL, 1.91 mmol) was added and stirring was continued at −35° C. After 30 min, additional sodium hydride (27 mg, 0.40 mmol) and 2,2,2-trifluoroethyl trichloromethanesulfonate (0.140 mL, 0.85 mmol) were added. After 2 h, the reaction was quenched with H2O and the mixture was extracted with EtOAc. The organic layer was washed with water (3×), then brine, then dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—100:0 to 70:30, to give the title compound. MS: m/z=423 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390798B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-a885a7f6fcbd4be390bc07607be3d3f1
출처 메모uspto-grants-2008_06