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HRID 19678作成日:2026年10月26日
Citric Acid → 6-fluoro-4-hydroxy-4-phenyl-3-(2,2,2-trifluoroethyl)-3,4-dihydroquinazolin-2(1H)-one
https://huagongshe.com/reaction/19678
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Citric Acid | HCID 311 | — |
| 反応物 | Ethanamine, 2,2,2-trifluoro- | HCID 9773 | — |
| 反応物 | Phosphorus oxide (P4O10) | HCID 14812 | — |
| 反応物 | N-(2-benzoyl-4-fluorophenyl)-1H-imidazole-1-carboxamide | HCID 21755401 | — |
| 溶媒 | Butyl Chloride | HCID 8005 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 6-fluoro-4-hydroxy-4-phenyl-3-(2,2,2-trifluoroethyl)-3,4-dihydroquinazolin-2(1H)-one | HCID 59346581 | — |
反応手順
To a suspension of N-(2-benzoyl-4-fluorophenyl)-1H-imidazole-1-carboxamide (30.00 g, 97.00 mmol) in THF (300 mL) was added 2,2,2-trifluoroethylamine (11.53 g, 116.39 mmol). The reaction was heated to 50° C. After 19 h at 50° C., the reaction was cooled to ambient temperature. Butyl chloride (500 mL) and 10% citric acid (250 mL) were added and the reaction stirred vigorously for 40 min. The precipitate was then isolated by vacuum filtration and placed under vacuum alongside P2O5 for 16 h to give 6-fluoro-4-hydroxy-4-phenyl-3-(2,2,2-trifluoroethyl)-3,4-dihydroquinazolin-2(1H)-one as a yellow solid. 1H NMR (CDCl3, 400 MHz) 8.59 (s, NH); d (7.47, J=6.96 Hz, 2H, ArH); 7.36 (m, 3H, ArH); 6.99 (m, 2H, ArH); 6.79 (m, 1H, ArH); 4.39 (m, 1H, CH2); 3.56 (m, 1H, CH2); 3.23 (s, OH); MS (Electrospray): m/z 363.0 (M+Na).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07745452B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-cb17f4f1b228495ebad976dd6cb81542 |
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| 出典メモ | uspto-grants-2010_06 |
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