돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1290702생성일: 2026년 10월 26일

Water → Benzyl (2-oxo-5-phenyl-2,3-dihydro-1h-benzo[e][1,4]diazepin-3-yl)carbamate

https://huagongshe.com/reaction/1290702

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium sodium tartarateHCID 9855836—
반응물Ammonium cerium (IV) nitrateHCID 9869224—
반응물(+/-) 3-[N-carbobenzyloxy]amino-2,3-dihydro-1-[4-methoxybenzyl]-2-oxo-5-phenyl-1H-1,4-benzodiazepineHCID 18917688—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물Benzyl (2-oxo-5-phenyl-2,3-dihydro-1h-benzo[e][1,4]diazepin-3-yl)carbamateHCID 2756242—

반응 단계

A suspension of (±) 3-[N-carbobenzyloxy]amino-2,3-dihydro-1-[4-methoxybenzyl]-2-oxo-5-phenyl-1H-1,4-benzodiazepine (0.58 g, 1.15 mmol, from step 5 of Example 1) in a mixture of acetonitrile (3.3 mL), water (1.2 mL) and ammonium cerium(IV) nitrate (3.1 g) was vortexed vigorously for 5 minutes. The resultant clear orange solution was stirred at room temperature for 20 minutes and add dropwisely into a mixture of saturated sodium potassium tartrate solution (40 mL), water (27 mL), and ethyl acetate (190 mL). The resultant mixture was stirred at room temperature for 1.5 hour, and the organic extract was washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated under vacuo. The residue was subjected to column chromatography on silica gel eluting with 2% methanol in chloroform. Collection and concentration of appropriate fraction provided the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05753650
출처 데이터셋uspto-grants-1998_05
ORD IDord-dc64e52ecc43483fa1c80890a2726cb6
출처 메모uspto-grants-1998_05