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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 658193생성일: 2026년 10월 23일

Stannous Chloride → 6-Amino-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-carboxamide

https://huagongshe.com/ko/reaction/658193

반응식

참여 물질

역할이름HCID투입량
반응물Stannous ChlorideHCID 24479—
반응물N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-nitro-1-benzofuran-2-carboxamideHCID 59341358—
용매DimethylformamideHCID 6228—
생성물6-Amino-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-carboxamideHCID 59341434—

반응 단계

15.0 ml (30 mmol) of a 2 M tin(II) chloride solution in DMF are added to N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-nitro-1-benzofuran-2-carboxamide (1550 mg, 4.92 mmol). The mixture is stirred overnight. The solvent is removed under reduced pressure using a rotary evaporator. The crude product is taken up in methanol and, together with acidic ion exchange resin (Dowex WX2-200), shaken for about 1 h. The loaded ion exchanger is washed with methanol, then with water, DMF, again with methanol, with dichloromethane and finally again with methanol. The product is eluted with methanol/triethylamine 95:5. The solvent is removed under reduced pressure using a rotary evaporator. The crude product is purified on silica gel 60 (mobile phase: dichloromethane/triethylamine 100:1→dichloro-methane/methanol/triethylamine 100:1:1→dichloromethane/methanol/triethylamine 90:10:1). 643 mg (46% 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-6281bb043fa5453c8000b70327066ec7
출처 메모uspto-grants-2011_12