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Ethyl 2-aminothiazole-4-carboxylate → Ethyl 6-(2-nitrophenyl)imidazo[2,1-b]thiazole-3-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl 2-aminothiazole-4-carboxylate | HCID 73216 | — |
| 反応物 | 2-Bromo-2'-nitroacetophenone | HCID 244025 | — |
| 溶媒 | Methyl Ethyl Ketone | HCID 6569 | — |
| 生成物 | Ethyl 6-(2-nitrophenyl)imidazo[2,1-b]thiazole-3-carboxylate | HCID 25232522 | 79.4% |
反応手順
In a typical run, 2.1 g of ethyl 2-aminothiazole-4-carboxylate (Combi-Blocks, 0.0123 mol) was mixed with 25 mL of methyl ethyl ketone along with 2-bromo-2′-nitroacetophenone (3.0 g, 0.0123 mol). The reaction mixture was stirred under reflux for 18 hours. It was then cooled to room temperature and filtered to remove some of the solids. The filtrate was concentrated to afford 3.10 g of 6-(2-nitro-phenyl)-imidazo[2,1-b]thiazole-3-carboxylic acid ethyl ester (MS, M++H=318).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08088928B2 |
| 出典データセット | uspto-grants-2012_01 |
| ORD ID | ord-f11f0e9818664a20991016afb4914dc7 |
| 出典メモ | uspto-grants-2012_01 |