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HRID 562030作成日:2026年10月27日

Triethylamine → 5-bromo-3-{1-[(1-methylethyl)sulfonyl]-4-piperidinyl}-1H-indole-7-carboxamide

https://huagongshe.com/reaction/562030

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-Propanesulfonyl chlorideHCID 82408—
反応物5-bromo-3-(4-piperidinyl)-1H-indole-7-carboxamide hydrochlorideHCID 66723284—
溶媒DimethylformamideHCID 6228—
溶媒Water ethylacetateHCID 22728543—
生成物5-bromo-3-{1-[(1-methylethyl)sulfonyl]-4-piperidinyl}-1H-indole-7-carboxamideHCID 5773262775%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063071B2
出典データセットuspto-grants-2011_11
ORD IDord-790a62cb8ee143c486885e2076fdd8d9
出典メモuspto-grants-2011_11