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1-benzyl-1H-imidazole-2-carbaldehyde → 6-[2-(1-Benzylimidazol-2-yl)vinyl]-2-ethylaminobenzoxazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-benzyl-1H-imidazole-2-carbaldehyde | HCID 139082 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 反応物 | [2-(N-ethylformamido)benzoxazol-6-yl]-methyltriphenylphosphonium bromide | HCID 86745044 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 6-[2-(1-Benzylimidazol-2-yl)vinyl]-2-ethylaminobenzoxazole | HCID 54324006 | 63.3% |
反応手順
A mixture of [2-(N-ethylformamido)benzoxazol-6-yl]-methyltriphenylphosphonium bromide (0.5 g), 1-benzyl-2-imidazolecarbaldehyde (0.2 g) and potassium tert-butoxide (0.1 g) in tetrahydrofuran (5.0 ml) was refluxed for 50 minutes. Evaporation of a solvent gave a residue, which was purified by a column chromatography on silica gel eluting with a mixture of chloroform and methanol (19:1, V/V). The eluted fractions containing the desired product were collected and evaporated in vacuo to give 6-[2-(1-benzylimidazol-2-yl)vinyl]-2-ethylaminobenzoxazole (0.2 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05047411 |
| 出典データセット | uspto-grants-1991_09 |
| ORD ID | ord-5278b472a91b4f3f8c1b2079ffd73702 |
| 出典メモ | uspto-grants-1991_09 |