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Triethylamine → 5-bromo-3-{1-[(1-methylethyl)sulfonyl]-4-piperidinyl}-1H-indole-7-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2-Propanesulfonyl chloride | HCID 82408 | — |
| 反応物 | 5-bromo-3-(4-piperidinyl)-1H-indole-7-carboxamide hydrochloride | HCID 66723284 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Water ethylacetate | HCID 22728543 | — |
| 生成物 | 5-bromo-3-{1-[(1-methylethyl)sulfonyl]-4-piperidinyl}-1H-indole-7-carboxamide | HCID 57732627 | 75% |
反応手順
Triethylamine (2.6 mL, 18.7 mmol) was added to a solution of 5-bromo-3-(4-piperidinyl)-1H-indole-7-carboxamide hydrochloride in DMF (15 mL) at 0° C. The mixture was stirred at room temperature for 10 min, and 2-propanesulfonyl chloride (1.04 mL, 9.32 mmol) was added. Stirring continued for another 30 min, and the reaction mixture was diluted with 1:1 EtOAc/H2O (200 mL). The layers were separated, and the aqueous layer was extracted with EtOAc (2×50 mL). The combined organic layers were washed with saturated NaCl (1×100 mL), dried (MgSO4), and concentrated under reduced pressure. The crude product was washed with MeOH (2×10 mL) to give the title compound (1.5 g, 75%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08063071B2 |
| 出典データセット | uspto-grants-2011_11 |
| ORD ID | ord-790a62cb8ee143c486885e2076fdd8d9 |
| 出典メモ | uspto-grants-2011_11 |