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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218478Generated: October 25, 2026

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

https://huagongshe.com/reaction/218478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-bromo-1H-indazole-3-carboxylateHCID 12689298—
ReactantHCID 178526064HCID 178526064—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Productmethyl 5-formyl-1H-indazole-3-carboxylateHCID 2495874554%

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198456B2
Source datasetuspto-grants-2012_06
ORD IDord-ad5e6f2faee44796820de143999deeae
Source noteuspto-grants-2012_06