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HRID 1713972作成日:2026年10月26日
2-Thiophenecarbonyl chloride → N-(3-Morpholinopropyl)-N-(4-(3-phenylisoxazol-5-yl)thiazol-2-yl)thiophene-2-carboxamide
https://huagongshe.com/reaction/1713972
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Thiophenecarbonyl chloride | HCID 78928 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 5-(Bromoacetyl)-3-phenylisoxazole | HCID 2735532 | — |
| 反応物 | N-[3-(4-Morpholinyl)propyl]thiourea | HCID 2760135 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | N-(3-Morpholinopropyl)-N-(4-(3-phenylisoxazol-5-yl)thiazol-2-yl)thiophene-2-carboxamide | HCID 59769689 | 53.8% |
反応手順
A mixture of 2-bromo-1-(3-phenylisoxazol-5-yl)ethan-1-one (160 mg, 0.6 mmol) and (3-morpholin-4-yl-propyl)-thiourea (122 mg, 0.6 mmol) in dry dioxane (5 ml) was heated at 80° C. for 2 h, cooled to room temperature, and concentrated in vacuo. The resulting residue was suspended in dichloromethane (5 mL) followed by the addition of N,N-diisopropylethylamine (209 μL, 1.2 mmol) and thiophene-2-carbonyl chloride (96 μL, 0.9 mmol). The reaction mixture was maintained at room temperature overnight, then concentrated in vacuo. The resulting residue was dissolved in DMSO (2.5 mL) and subjected to HPLC purification (Method Y). The resulting free amine was dissolved in MeOH (1 mL) and 1M HCl/ether (50 mL) was added. The precipitate was filtered and dried in vacuo to provide the title compound (155 mg) as an off-white solid as the hydrochloride salt. LC/MS (ESI) m/z 481.1 [M+H]. HPLC retention time (Method B)=2.94 min.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07795290B2 |
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| 出典データセット | uspto-grants-2010_09 |
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| ORD ID | ord-0d95d6129f614471822fbaaf9c876d53 |
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| 出典メモ | uspto-grants-2010_09 |
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