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HRID 527444作成日:2026年10月27日

Water → methyl 2-(1-(4-chlorobenzoyl)-5-methoxy-1H-indol-3-yl)acetate

https://huagongshe.com/reaction/527444

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物4-Chlorobenzoyl chlorideHCID 8501—
反応物Sodium hydrideHCID 24758—
反応物methyl 2-(5-methoxy-1H-indol-3-yl)acetateHCID 594955—
溶媒DimethylformamideHCID 6228—
生成物methyl 2-(1-(4-chlorobenzoyl)-5-methoxy-1H-indol-3-yl)acetateHCID 57563309—

反応手順

Methyl 2-(5-methoxy-1H-indol-3-yl)acetate (60 mg, 0.27 mmol) and NaH (8 mg, 0.33 mmol) were stirred in anhydrous DMF (1 mL) at 0° C. under argon for 30 min, at which time 4-chlorobenzoyl chloride (57 mg, 0.33 mmol) was added. The reaction mixture was stirred overnight at room temperature and was then poured into cold water (2 mL). The organic compound was immediately extracted with dichloromethane (2×2 mL), dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified on silica (ethyl acetate/hexane gradient) and recrystallized from hexane. Yield: 18 mg (18%). C19H16ClNO4, Mr=357.79; 1H NMR (400 MHz, DMSO-d6) d: 3.61 (s, 3H), 3.78 (s, 2H), 3.81 (s, 3H), 7.00 (dd, J=2.4/9.0 Hz, 1H), 7.12 (d, J=2.4 Hz, 1H), 7.35 (s, 1H), 7.65-7.77 (m, 4H), 8.17 (d, J=8.8 Hz, 1H); LCMS (ESI) tR: 2.81 min (>99%, ELSD), m/z: 358.0 [M+1]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09346803B2
出典データセットuspto-grants-2016_05
ORD IDord-64547cd1dbe042d9896b7a22cb3b889b
出典メモuspto-grants-2016_05