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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133129생성일: 2026년 10월 23일

1,2-Dichloroethane → tert-Butyl [(3R,6S)-6-(2,3-difluorophenyl)-2-oxoazepan-3-yl]carbamate

https://huagongshe.com/ko/reaction/133129

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물TriethylamineHCID 8471—
반응물HOAtHCID 181649—
반응물Sodium BicarbonateHCID 516892—
반응물(5S)-N2,N2-Bis(tert-butoxycarbonyl)-5-(2,3-difluorophenyl)-D-lysineHCID 67526479—
용매DichloromethaneHCID 6344—
생성물tert-Butyl [(3R,6S)-6-(2,3-difluorophenyl)-2-oxoazepan-3-yl]carbamateHCID 23657400—

반응 단계

To a solution (5S)—N2,N2-bis(tert-butoxycarbonyl)-5-(2,3-difluorophenyl)-D-lysine from Step D (22.0 g, 48.0 mmol) in CH2Cl2 (700 mL) were added EDC (11.0 g, 57.6 mmol) and HOAT (3.27 g, 24.0 mmol) followed by triethylamine (10.0 mL, 72.0 mmol). After 1 h, aqueous NaHCO3 was added, the layers were separated, and the aqueous phase was extracted with CH2Cl2. The combined organic extracts were dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by silica gel chromatography, eluting with CH2Cl2:MeOH—90:10, to give the title compound. MS: m/z=341 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390798B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-558f8849205643dfa6130d05bee5202e
출처 메모uspto-grants-2008_06