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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 335591생성일: 2026년 10월 24일

Stannous Chloride → N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-amino-1-benzofuran-2-carboxamide

https://huagongshe.com/ko/reaction/335591

반응식

참여 물질

역할이름HCID투입량
반응물Stannous ChlorideHCID 24479—
반응물N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-nitro-1-benzofuran-2-carboxamideHCID 59341430—
용매DimethylformamideHCID 6228—
생성물N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-amino-1-benzofuran-2-carboxamideHCID 59341406—

반응 단계

6.0 ml (12 mmol) of a 2 M tin(II) chloride solution in DMF are added to N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-nitro-1-benzofuran-2-carboxamide (1340 mg, 4.25 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, again with methanol, with DMF, again with methanol, with THF, again with methanol, with dichloromethane and finally once more with methanol. The product is eluted with methanol/triethylamine 95:5. The solvent is removed under reduced pressure using a rotary evaporator. 1200 mg (98% of theory) of the title compound are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08884017B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-3e4bf6b604ba4fb2b9d0a2ae38dcff94
출처 메모uspto-grants-2014_11