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Aminopyrazine → 2-(4-(3-(1-(Hydroxyimino)-2,3-dihydro-1h-inden-5-ylamino)imidazo[1,2-a]pyrazin-2-yl)phenoxy)-n-methylacetamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Aminopyrazine | HCID 78747 | — |
| 反応物 | 2-(4-formylphenoxy)-N-methylacetamide | HCID 15270519 | — |
| 反応物 | 5-isocyano-2,3-dihydroinden-1-one O-tert-butyldimethylsilyl oxime | HCID 57762062 | — |
| 触媒 | Scandium(III) triflate | HCID 2734571 | — |
| 溶媒 | Dichloromethane methanol | HCID 21226129 | — |
| 生成物 | 2-(4-(3-(1-(Hydroxyimino)-2,3-dihydro-1h-inden-5-ylamino)imidazo[1,2-a]pyrazin-2-yl)phenoxy)-n-methylacetamide | HCID 137194567 | — |
反応手順
A mixture of pyrazin-2-amine (12) (1.1 eq.), 2-(4-formylphenoxy)-N-methylacetamide (9) (1.1 eq.) and a catalytic amount of Sc(OTf)3 was stirred in 2 mL of 1:1 DCM/MeOH at room temperature for 30 minutes. To this was added 5-isocyano-2,3-dihydroinden-1-one O-tert-butyldimethylsilyl oxime (1 eq.) as a 2 mL solution in 1:1 DCM/MeOH and the mixture was stirred at room temperature for 18 hours. The reaction mixture was then concentrated under vacuum and the residue taken up in EtOAc (with a small amount of methanol added to help with dissolution) and purified by column using 1-5% MeOH/EtOAc+1% NH4OH. The desired product (14) was isolated as a light yellow solid. MS (APCI) m/z 443.1 (M+1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07566716B2 |
| 出典データセット | uspto-grants-2009_07 |
| ORD ID | ord-96fcc8a891764c2cbf2c88da8dd3c11d |
| 出典メモ | uspto-grants-2009_07 |