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HRID 39051作成日:2026年10月25日

Potassium Carbonate → 3-Cyclohexyl-2-[2-(2,4-dimethyl-thiazol-5-yl)-quinolin-6-yl]-1H-indole-6-carboxylic acid methyl ester

https://huagongshe.com/reaction/39051

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2-bromo-1H-indoleHCID 11805631—
反応物Toluene ethanolHCID 21863594—
反応物[2-(2,4-Dimethyl-1,3-thiazol-5-yl)quinolin-6-yl]boronic acidHCID 58710276—
生成物3-Cyclohexyl-2-[2-(2,4-dimethyl-thiazol-5-yl)-quinolin-6-yl]-1H-indole-6-carboxylic acid methyl esterHCID 5871032767%

反応手順

A mixture of intermediate 1-5 (4.02 g, 12 mmol), 2-(2,4-dimethyl-thiazol-5-yl)-quinoline-6-boronic acid 16-1 (4.58 g, 1.19 eq, synthesized as described in WO2006/076529), K2CO3 (5.13 g, 3.1 eq) and dichloro-bis(triphenylphosphino)-Pd(II) (0.86 g, 0.10 eq) in ethanol/toluene (1:1, 80 mL) was stirred at room temperature under N2 overnight. After concentration under reduced pressure, the reaction mixture was redissolved in ethyl acetate and washed with a 5 M NaHCO3 solution. The obtained yellow precipitate was filtered off, washed with water, then isopropanol to give 4.13 g (67%) of 3-Cyclohexyl-2-[2-(2,4-dimethyl-thiazol-5-yl)-quinolin-6-yl]-1H-indole-6-carboxylic acid methyl ester 16-2 as a yellow solid; m/z=496 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524716B2
出典データセットuspto-grants-2013_09
ORD IDord-31a5f6617cc94964ace8891f9b4eb27f
出典メモuspto-grants-2013_09