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HRID 1748438作成日:2026年10月26日

Hydrochloric Acid → 1-{5-[(1E)-3-Methoxy-1-propenyl]pyridin-2-yl}-5-methyl-1H-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/1748438

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium HydroxideHCID 14798—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
反応物Ethyl 1-(5-bromopyridin-2-yl)-5-methylpyrazole-4-carboxylateHCID 46739344—
反応物3-Methoxy-1-propenylboronic acid pinacol esterHCID 53399113—
触媒palladium(II) acetateHCID 167845—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物1-{5-[(1E)-3-Methoxy-1-propenyl]pyridin-2-yl}-5-methyl-1H-pyrazole-4-carboxylic acidHCID 86692408549.6%

反応条件

温度100 °C

反応手順

Tetrahydrofuran (4 ml) was added to 1-(5-bromopyridin-2-yl)-5-methyl-1H-pyrazole-4-carboxylic acid ethyl ester (620 mg) described in Reference Example 24(2), palladium (II) acetate (45 mg), 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (S-Phos) (82 mg), 3-methoxy-1-propenylboronic acid pinacol ester (594 μl) and tripotassium phosphate (1.0 g), and stirred at 100° C. for 4.5 hours. Then, water (5 ml), 4N aqueous solution of sodium hydroxide (5 ml) and ethanol (5 ml) were added to the reaction solution and the mixture was stirred at 80° C. for two hours. The reaction solution was acidified by the addition of water and 1N hydrochloric acid aqueous solution, extracted with ethyl acetate and the solvent was evaporated in vacuo. The resulting solid was washed with water to give the titled compound (300 mg) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09150555B2
出典データセットuspto-grants-2015_10
ORD IDord-1a573bd2686a4f079c7d88279b015f26
出典メモuspto-grants-2015_10