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N-{[5-(2-chloroacetyl)furan-2-yl]methyl}acetamide → 4-(5-Acetylaminomethylfuran-2-yl)-2-(diaminomethyleneamino)thiazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N-{[5-(2-chloroacetyl)furan-2-yl]methyl}acetamide | HCID 2393628 | — |
| 反応物 | Amidinothiourea | HCID 2724563 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 4-(5-Acetylaminomethylfuran-2-yl)-2-(diaminomethyleneamino)thiazole | HCID 11778366 | 46.6% |
反応手順
A solution of 5-acetylaminomethyl-2-chloroacetylfuran (39.9 g) and diaminomethylenethiourea (21.9 g) in ethanol (400 ml) was refluxed for two hours with stirring. The solvent was evaporated in vacuo and the residue was dissolved in water (300 ml). The solution was basified with an aqueous potassium carbonate. The resulting precipitate was collected by filtration, washed with water and recrystallized from a mixture of methanol, tetrahydrofuran and diisopropyl ether to afford 4-(5-acetylaminomethylfuran-2-yl)-2-(diaminomethyleneamino)thiazole (24.1 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05308857 |
| 出典データセット | uspto-grants-1994_05 |
| ORD ID | ord-8a22acb0dcf145649c406210ab4bf3a1 |
| 出典メモ | uspto-grants-1994_05 |