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HRID 2377682作成日:2026年10月26日

5-Fluoroindole-2-carboxylic acid → 5-fluoro-2-{[4-(2-pyridinyl)-1-piperazinyl]carbonyl}-1H-indole

https://huagongshe.com/reaction/2377682

反応式

関与物質

役割名称HCID仕込み量
反応物5-Fluoroindole-2-carboxylic acidHCID 1820—
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物1-(2-Pyridyl)piperazineHCID 94459—
溶媒DichloromethaneHCID 6344—
生成物5-fluoro-2-{[4-(2-pyridinyl)-1-piperazinyl]carbonyl}-1H-indoleHCID 22065982—

反応条件

温度25 °C

反応手順

5-Fluoro-1H-indole-2-carboxylic acid (4.0 g) and EDCI (4.29 g) were combined in dichloromethane (90 mL) and treated with 1-(2-pyridinyl)piperazine (3.64 g). After stirring at 25° C. for 24 hours, the mixture was washed with 150 mL of water and filtered. The filter cake was washed in succession with 300 mL of water, 250 mL of dichloromethane and 20 mL of ethyl acetate to provide the title compound. 1H NMR (d6-DMSO, 300 MHz) δ 3.61 (m, 4H), 3.85 (m, 4H), 6.67 (dd, 1H, J=7.5, 4.8 Hz), 6.85 (m, 2H), 7.06 (m, 1H), 7.40 (m, 2H), 7.65 (m, 1H), 8.04 (dd, 1H, J=4.5, 1.8 Hz), 11.72 (bs, 1H). MS (DCI/NH3) m/z 325 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07470691B2
出典データセットuspto-grants-2008_12
ORD IDord-29545119b5524fe79ef5e1760a144afd
出典メモuspto-grants-2008_12