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HRID 43005作成日:2026年10月23日
Potassium Carbonate → (S)-N-(5-((3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl)methyl)-2,3-dihydro-1H-inden-2-yl)propane-2-sulfonamide
https://huagongshe.com/ja/reaction/43005
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | 3-(Trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazole | HCID 2802863 | — |
| 反応物 | (S)-N-(5-(hydroxymethyl)-2,3-dihydro-1H-inden-2-yl)propane-2-sulfonamide | HCID 67088215 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (S)-N-(5-((3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl)methyl)-2,3-dihydro-1H-inden-2-yl)propane-2-sulfonamide | HCID 53323974 | 3.1% |
反応手順
(S)—N-(5-(hydroxymethyl)-2,3-dihydro-1H-inden-2-yl)propane-2-sulfonamide (23 mg, 0.086 mmol) was dissolved in DCM (5 mL) and thionyl chloride (51 mg, 0.43 mmol) was added. The reaction mixture was stirred at room temperature for 1 h before being concentrated to dryness. The whole was dissolved in DMF (2 mL) to this was added 3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazole (25 mg, 0.086 mmol) followed by potassium carbonate (24 mg, 0.172 mmol). The reaction mixture was heated to 65° C. for 3 h before being quenched with water (2 mL) and the organics extracted with EtOAc (3×5 mL). The combined organics were washed with brine, dried (MgSO4) and concentrated under reduced pressure. Purification by preparative basic HPLC gave the title compound (1.2 mg, 2.7 μmol, 2.9%). MS (ESI): m/z [M+H]+ 442.2
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08536214B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-4ffbad2175c947f6baca2627d80488fa |
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| 出典メモ | uspto-grants-2013_09 |
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