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HRID 854799作成日:2026年10月27日
Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) → 3-(3-hydroxy-cyclopentyl)-2-(4-methanesulfonyl-phenyl)-N-thiazol-2-yl-propionamide
https://huagongshe.com/reaction/854799
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| 反応物 | 2-(4-methanesulfonyl-phenyl)-3-[3-(tetrahydropyran-2-yloxy)-cyclopentyl]-N-thiazol-2-yl-propionamide | HCID 21958965 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 3-(3-hydroxy-cyclopentyl)-2-(4-methanesulfonyl-phenyl)-N-thiazol-2-yl-propionamide | HCID 9977954 | 86% |
反応手順
A solution of 2-(4-methanesulfonyl-phenyl)-3-[3-(tetrahydropyran-2-yloxy)-cyclopentyl]-N-thiazol-2-yl-propionamide (450 mg, 0.94 mmol) in ethanol (9.4 mL) was treated with pyridinium p-toluenesulfonate (24 mg, 0.094 mmol). The resulting reaction mixture was heated at 60° C. for 4 h. The reaction mixture was allowed to cool to 25° C. and then concentrated in vacuo. The resulting yellow residue was diluted with ethyl acetate (100 mL) and then washed with a saturated aqueous sodium chloride solution. The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 1/3 to 1/7 hexanes/ethyl acetate) afforded the 3-(3-hydroxy-cyclopentyl)-2-(4-methanesulfonyl-phenyl)-N-thiazol-2-yl-propionamide (318 mg, 86%) as a white foam: mp 69-72° C.; FAB-HRMS m/e calcd for C18H22N2O4S2 (M+H)+ 395.1099. found 395.1091.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07259166B2 |
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| 出典データセット | uspto-grants-2007_08 |
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| ORD ID | ord-efa828573b1e4a419f60a71d422d2d21 |
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| 出典メモ | uspto-grants-2007_08 |
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