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HRID 335591作成日:2026年10月25日

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

https://huagongshe.com/reaction/335591

反応式

関与物質

役割名称HCID仕込み量
反応物Stannous ChlorideHCID 24479—
反応物N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-nitro-1-benzofuran-2-carboxamideHCID 59341430—
溶媒DimethylformamideHCID 6228—
生成物N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-amino-1-benzofuran-2-carboxamideHCID 59341406—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08884017B2
出典データセットuspto-grants-2014_11
ORD IDord-3e4bf6b604ba4fb2b9d0a2ae38dcff94
出典メモuspto-grants-2014_11