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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404680Generated: October 31, 2026

2-Pyridinecarboxaldehyde → HCID 178419322, compound

https://huagongshe.com/reaction/1404680

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PyridinecarboxaldehydeHCID 14273—
Reactant4-Bromobenzene-1,2-diamineHCID 323593—
ReactantSodium BisulfiteHCID 23665763—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178419322HCID 17841932240.5%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 4-bromo-1,2-diaminobenzene (1.00 g, 5.35 mmol), sodium bisulfite (1.02 g) in water (8 mL) and ethanol (80 mL) and 2-pyridine carboxaldehyde (0.63 g, 5.88 mmol) was heated at 90° C. for 15 h. The reaction was cooled to room temperature and concentrated under vacuum. The residue was partitioned between water (60 mL) and chloroform (80 mL) and the aqueous phase was extracted with chloroform (2×50 mL). The organic extracts were combined, dried (MgSO4), filtered and concentrated under vacuum to give the crude product (1.36 g). The residue was purified by column chromatography eluting with EtOAc:hexaxes 0 to 50% to afford 594 mg of 5-bromo-2-(pyridin-2-yl)-1H-benzo[d]imidazole (40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912336B2
Source datasetuspto-grants-2014_12
ORD IDord-38ac2725cbc2442bb6994e4bdaa5c35c
Source noteuspto-grants-2014_12