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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 963465생성일: 2026년 10월 25일

N-tert-Butoxycarbonyl-L-tryptophan → (3S)-3-amino-1-{(3-azabicyclo[3.2.2]non-3-yl)carbonylmethyl}-2,3-dihydro-5-(2-fluorophenyl)-1H-1,4-benzodiazepin-2-one

https://huagongshe.com/reaction/963465

반응식

참여 물질

역할이름HCID투입량
반응물N-tert-Butoxycarbonyl-L-tryptophanHCID 83169—
반응물(3RS)-1-{(3-azabicyclo[3.2.2]non-3-yl)-carbonylmethyl}-3-amino-5-(2-fluorophenyl)-2,3-dihydro-1H-1,4-benzodiazepin-2-oneHCID 19081160—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
생성물(3S)-3-amino-1-{(3-azabicyclo[3.2.2]non-3-yl)carbonylmethyl}-2,3-dihydro-5-(2-fluorophenyl)-1H-1,4-benzodiazepin-2-oneHCID 5442502146%

반응 단계

To a solution of N-tert-butoxycarbonyl-L-tryptophan (0.70 g) in acetonitrile (20 ml) was added dropwise a solution of (3RS)-3-amino-1-{(3-azabicyclo[3.2.2]non-3-yl)carbonylmethyl}-2,3-dihydro-5-(2-fluorophenyl)-1H-1,4-benzodiazepin-2-one (1.00 g) in methylene chloride (5 ml) under stirring at ambient temperature. The mixture was stirred overnight. The precipitate was collected by filtration and the colorless solid was partitioned between methylene chloride and 0.5N NaOH. The organic layer was dried over sodium sulfate, filtered and concentrated in vacuo to afford (3S)-3-amino-1-{(3-azabicyclo[3.2.2]non-3-yl)carbonylmethyl}-2,3-dihydro-5-(2-fluorophenyl)-1H-1,4-benzodiazepin-2-one (0.46 g) as s colorless crystal.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05763437
출처 데이터셋uspto-grants-1998_06
ORD IDord-b138eac3035940ed844fdebad43ac9a4
출처 메모uspto-grants-1998_06