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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1714468생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1714468

반응식

참여 물질

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

반응 단계

1.55 g (4.92 mmol) of N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-nitro-1-benzofuran-2-carboxamide are dissolved in 15 ml of 2 M tin(II) chloride solution in DMF and stirred at room temperature overnight. Dowex 50WX2-200 ion exchanger resin is added and, within 1 h, the mixture is concentrated in a rotary evaporator. The resin is washed successively with water, DMF, methanol, dichloromethane, methanol and 10% triethylamine in methanol. The product fraction is concentrated and chromatographed on silica gel (mobile phase: dichloromethane/methanol/triethylamine). Concentration in vacuo results in 642.8 mg (45.8% of theory) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07795453B2
출처 데이터셋uspto-grants-2010_09
ORD IDord-a6af2ecee7e04d4a8c0bc20ef0c9f3b5
출처 메모uspto-grants-2010_09