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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218463Generated: October 29, 2026

Sodium Formate → 3-(1H-benzimidazol-2-yl)-1H-indazole-5-carboxaldehyde

https://huagongshe.com/reaction/218463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium FormateHCID 2723810—
Reactant3-(1H-Benzo[D]imidazol-2-YL)-5-iodo-1H-indazoleHCID 135971798—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3-(1H-benzimidazol-2-yl)-1H-indazole-5-carboxaldehydeHCID 13597179737%

Reaction Conditions

Temperature90 °C

Reaction Steps

3-(1H-benzimidazol-2-yl)-5-iodo-1H-indazole (500 mg, 1.39 mmol) was dissolved in DMF (5 mL), then Pd(PPh3)2Cl2 (24 mg, 0.034 mmol) and sodium formate (142 mg, 2.1 mmol) were added. The reaction mixture was put under vacuum and recharged with CO three times, then heated up to 90° C. for 4 hr. The mixture was diluted with EtOAc, washed with brine, dried and concentrated. The crude product was purified by flash chromatography to afford 3-(1H-benzimidazol-2-yl)-1H-indazole-5-carboxaldehyde (135 mg, 37%) as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198456B2
Source datasetuspto-grants-2012_06
ORD IDord-3c75f4f93bc749b98db430601a9902e9
Source noteuspto-grants-2012_06