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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20179생성일: 2026년 10월 23일

2,3-Difluorobenzaldehyde → tert-Butyl 1-(2,3-difluorobenzyl)-5-oxo-4-(2,2,2-trifluoroethyl)-1,4-diazepan-6-ylcarbamate

https://huagongshe.com/ko/reaction/20179

반응식

참여 물질

역할이름HCID투입량
반응물2,3-DifluorobenzaldehydeHCID 137664—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물tert-Butyl 7-oxo-1-(2,2,2-trifluoroethyl)-1,4-diazepan-6-ylcarbamateHCID 66939478—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
생성물tert-Butyl 1-(2,3-difluorobenzyl)-5-oxo-4-(2,2,2-trifluoroethyl)-1,4-diazepan-6-ylcarbamateHCID 6843300788.6%

반응 단계

A mixture of tert-butyl 7-oxo-1-(2,2,2-trifluoroethyl)-1,4-diazepan-6-ylcarbamate (51 mg, 0.16 mmol), 2,3-difluorobenzaldehyde (0.053 mL, 0.49 mmol), and sodium cyanoborohydride (31 mg, 0.49 mmol) in methanol (5 mL) was adjusted to pH 4 with acetic acid. After 0.5 h, saturated aqueous sodium bicarbonate was added and the mixture was extracted with dichloromethane (3×). The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated. Purification by silica gel chromatography [100% dichloromethane→95% dichloromethane/5% (10% ammonium hydroxide/methanol)] gave the title compound (62 mg). MS 438 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745427B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-01f51043ad52477d81f45ae29ff9fad2
출처 메모uspto-grants-2010_06