関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl benzoylacetate | HCID 7170 | — |
| 反応物 | Thiourea | HCID 2723790 | — |
| 反応物 | Hydroxy tosyloxy iodobenzene | HCID 21918218 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | Ethyl 2-amino-4-phenyl-1,3-thiazole-5-carboxylate | HCID 73239 | 75.9% |
反応手順
To a solution of ethyl 3-phenyl-3-oxopropionate (5.0 g, 26.0 mmol) in 100 mL of acetonitrile was added hydroxy(tosyloxy)iodobenzene (11.2 g, 28.6 mmol). The resulting suspension was stirred at 65° C. for 1 h at which time the reaction was a homogeneous solution. Thiourea (2.2 g, 28.6 mmol) was added and stirring was continued at 65° C. for 2 h. The mixture was cooled and concentrated, and the residue was taken up in ethyl acetate, washed with saturated aq Na2CO3 and brine, dried (MgSO4) and concentrated. The residue was triturated with ethyl ether to afford 4.9 g (70%) of the title compound as a yellow solid. 1H NMR (CDCl3) d 7.65 (m, 2H), 7.39 (m, 3H), 5.98 (broad s, 2H), 4.18 (q, 2H), 1.22 (t, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06602895B2 |
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| 出典データセット | uspto-grants-2003_08 |
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| ORD ID | ord-0f7ec75b59b14721884206e1f615b0c5 |
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| 出典メモ | uspto-grants-2003_08 |
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