돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 658190생성일: 2026년 10월 23일

Water → N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-5-amino-1-benzofuran-2-carboxamide

https://huagongshe.com/ko/reaction/658190

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium HydroxideHCID 14798—
반응물Stannous ChlorideHCID 24479—
반응물N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-5-nitro-1-benzofuran-2-carboxamideHCID 59341432—
용매DimethylformamideHCID 6228—
생성물N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-5-amino-1-benzofuran-2-carboxamideHCID 10236388—

반응 단계

2.0 ml (4 mmol) of a 2 M tin(II) chloride solution in DMF are added to N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-5-nitro-1-benzofuran-2-carboxamide (100 mg, 0.32 mmol). The mixture is stirred overnight. The reaction mixture is poured into water and made basic using 1N aqueous sodium hydroxide solution. The aqueous phase is extracted six times with ethyl acetate. The combined organic phases are dried over magnesium sulfate, and the solvent is removed under reduced pressure using a rotary evaporator. The crude product is taken up in methanol and shaken together with acidic ion exchange resin (Dowex WX2-200) for about 20 min. The loaded ion exchanger is washed three times with in each ase 30 ml of methanol, then with water/methanol 8:2, again with methanol, with dichloromethane and finally again with methanol. The product is eluted using methanol/triethylamine 95:5. The solvent is removed under reduced pressure using a rotary evaporator. 52 mg (58% of theory) of the title compound are isolated.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08076355B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-d3fb09c5c8384443a378647a8ad36b27
출처 메모uspto-grants-2011_12