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HRID 602137作成日:2026年10月26日
Water → Methyl 2-[3-[N-[[2-(4-chlorophenyl)-4-methylthiazol-5-yl]methyl]carbamoyl]piperidin-1-yl]benzoate
https://huagongshe.com/reaction/602137
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Benzoic acid, 2-fluoro-, methyl ester | HCID 67854 | — |
| 反応物 | N-[[2-(4-Chlorophenyl)-4-methylthiazol-5-yl]methyl]piperidine-3-carboxamide hydrochloride | HCID 67266868 | — |
| 溶媒 | Dimethyl Sulfoxide | HCID 679 | — |
| 生成物 | Methyl 2-[3-[N-[[2-(4-chlorophenyl)-4-methylthiazol-5-yl]methyl]carbamoyl]piperidin-1-yl]benzoate | HCID 58992625 | 4% |
反応手順
N-[[2-(4-Chlorophenyl)-4-methylthiazol-5-yl]methyl]piperidine-3-carboxamide hydrochloride (198 mg, 0.513 mmol) and methyl 2-fluorobenzoate (0.0653 mL, 0.513 mmol) were dissolved in dimethylsulfoxide (5 mL). To this solution, potassium carbonate (142 mg, 1.03 mmol) was added and the mixture was stirred for 6 hours at 160° C. Subsequently, the mixture was allowed to cool and water was added. The mixture was then extracted with ethyl acetate and the extract washed with brine, followed by drying over magnesium sulfate and evaporation of the solvent. Purification of the residue by silica gel column chromatography (hexane:ethyl acetate=5:1->1:1) gave 9.80 mg (4%) of the desired compound as a colorless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07902367B2 |
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| 出典データセット | uspto-grants-2011_03 |
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| ORD ID | ord-7e0fd348ca514ec39c1bb4ee8645f86b |
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| 出典メモ | uspto-grants-2011_03 |
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