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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 218460Erstellt: 25. Oktober 2026

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-iodo-N-methoxy-N-methyl-1H-indazole-3-carboxamideHCID 20580738—
EduktHCID 178526064HCID 178526064—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkt5-formyl-N-methoxy-N-methyl-1H-indazole-3-carboxamideHCID 2495874315,6%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08198456B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-0b44a3f09b694ce1b9e28c3b5e4698c1
Quellennotizuspto-grants-2012_06