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HRID 218460作成日:2026年10月27日

5-iodo-N-methoxy-N-methyl-1H-indazole-3-carboxamide → 5-formyl-N-methoxy-N-methyl-1H-indazole-3-carboxamide

https://huagongshe.com/reaction/218460

反応式

関与物質

役割名称HCID仕込み量
反応物5-iodo-N-methoxy-N-methyl-1H-indazole-3-carboxamideHCID 20580738—
反応物HCID 178526064HCID 178526064—
触媒HCID 178418476HCID 178418476—
溶媒DimethylformamideHCID 6228—
溶媒Sodium chloride; waterHCID 57417360—
生成物5-formyl-N-methoxy-N-methyl-1H-indazole-3-carboxamideHCID 2495874315.6%

反応手順

A mixture of 5-iodo-N-methoxy-N-methyl-1H-indazole-3-carboxamide (5 g, 15.1 mmol), HCOONa (1.85 g, 30.2 mmol), and PdCl2(PPh3)2 (320 mg, 0.453 mmol) in DMF (20 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. After cooling to rt, the reaction mixture was diluted with brine and extracted with EtOAc. The organic phases were combined, washed with brine, dried, and concentrated. The crude product was purified by column chromatography to afford 5-formyl-N-methoxy-N-methyl-1H-indazole-3-carboxamide (550 mg, 15.6%) as a white solid.

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-0b44a3f09b694ce1b9e28c3b5e4698c1
出典メモuspto-grants-2012_06