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1-[5-(2-Methyl-[1,3]dioxolan-2-yl)-furan-2-ylmethyl]-1H-pyrazol-3-ylamine → 2-(2-Methoxy-ethyl)-5-phenyl-oxazole-4-carboxylic acid [1-(5-acetyl-furan-2-ylmethyl)-1H-pyrazol-3-yl]-amide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-[5-(2-Methyl-[1,3]dioxolan-2-yl)-furan-2-ylmethyl]-1H-pyrazol-3-ylamine | HCID 66928781 | — |
| 反応物 | 2-(2-Methoxy-ethyl)-5-phenyl-oxazole-4-carboxylic acid | HCID 66928802 | — |
| 生成物 | 2-(2-Methoxy-ethyl)-5-phenyl-oxazole-4-carboxylic acid [1-(5-acetyl-furan-2-ylmethyl)-1H-pyrazol-3-yl]-amide | HCID 66928373 | — |
反応手順
Following general procedure B followed by C, starting from 1-[5-(2-methyl-[1,3]dioxolan-2-yl)-furan-2-ylmethyl]-1H-pyrazol-3-ylamine and 2-(2-methoxy-ethyl)-5-phenyl-oxazole-4-carboxylic acid. LC-MS-conditions 02: tR=1.0 min; [M+H]+=435.31.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08288419B2 |
| 出典データセット | uspto-grants-2012_10 |
| ORD ID | ord-756172fb5db9402490fe5be37d266de0 |
| 出典メモ | uspto-grants-2012_10 |