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HRID 218478作成日:2026年10月26日

Methyl 5-bromo-1H-indazole-3-carboxylate → methyl 5-formyl-1H-indazole-3-carboxylate

https://huagongshe.com/reaction/218478

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 5-bromo-1H-indazole-3-carboxylateHCID 12689298—
反応物HCID 178526064HCID 178526064—
触媒HCID 178418476HCID 178418476—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物methyl 5-formyl-1H-indazole-3-carboxylateHCID 2495874554%

反応手順

A mixture of 5-bromo-1H-indazole-3-carboxylic acid methyl ester (1 g, 3.92 mmol), HCOONa (400 mg, 5.88 mmol), and PdCl2(PPh3)2 (138 mg, 0.2 mmol) in DMF (10 mL) was put under vacuum, and charged with CO. This process was repeated three times, and the mixture was kept at 110° C. for 6 hr. The reaction mixture was cooled to rt, diluted with EtOAc and water, and extracted. The organic phase was dried and concentrated. Purification via flash chromatography afforded 5-formyl-1H-indazole-3-carboxylic acid methyl ester (430 mg, 54%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198456B2
出典データセットuspto-grants-2012_06
ORD IDord-ad5e6f2faee44796820de143999deeae
出典メモuspto-grants-2012_06