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HRID 2199752作成日:2026年10月25日

Cesium fluoride → 7-(2-Chlorophenyl)-3-(3-(ethyl(1-naphthyl)amino)propyl)-1h-indole-2-carboxylic acid

https://huagongshe.com/reaction/2199752

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium fluorideHCID 25953—
反応物2-Chlorophenylboronic acidHCID 2734322—
反応物Tri-tert-butylphosphine tetrafluoroborateHCID 2734635—
反応物Ethyl 7-bromo-3-(3-(ethyl(naphthalen-1-yl)amino)propyl)-1h-indole-2-carboxylateHCID 68938635—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒TetrahydrofuranHCID 8028—
生成物7-(2-Chlorophenyl)-3-(3-(ethyl(1-naphthyl)amino)propyl)-1h-indole-2-carboxylic acidHCID 68937151—

反応手順

To a mixture of EXAMPLE 531B (192 mg) and 2-chlorophenylboronic acid (76 mg) in tetrahydrofuran (6 ml) was added tris(dibenzylideneacetone)dipalladium(0) (19 mg), tri-t-butyl-phosphonium tetrafluoroborate (12 mg) and cesium fluoride (200 mg). The mixture was purged with argon and stirred at room temperature for 24 hours. The mixture was diluted with ethyl acetate (200 mL) and washed with water, and brine and dried over Na2SO4. Concentration of the mixture and column purification of the crude material (5% ethyl acetate in hexane) provided the title compound. A portion of this material (50 mg) was dissolved in 1:1 tetrahydrofuran/methanol with a few drops of water and hydrolyzed with LiOH. Subsequent purification via RP HPLC afforded the title compound. 1H NMR (300 MHz, DMSO-d6) δ 10.80 (m, 1H), 8.27 (m, 1H), 7.90 (m, 1H), 7.55 (m, 1H), 7.53 (m, 1H), 7.42 (m, 3H), 7.34 (m, 3H), 7.21 (m, 2H), 7.03 (m, 1H), 6.98 (m, 2H), 3.21 (m, 4H), 3.08 (t, 2H), 1.79 (m, 2H), 0.96 (t, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09359296B2
出典データセットuspto-grants-2016_06
ORD IDord-8e83260701dd45ff9a7eea08cebc7625
出典メモuspto-grants-2016_06