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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916664Generated: October 29, 2026

Glyoxal → 2-chloro-6-(1H-imidazol-2-yl)pyridine

https://huagongshe.com/reaction/916664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlyoxalHCID 7860—
ReactantAmmonium HydroxideHCID 14923—
Reactant6-Chloro-2-picolineHCID 87601—
Reactant6-Chloro-2-pyridinecarboxaldehydeHCID 10796848—
SolventMethanolHCID 887—
Product2-chloro-6-(1H-imidazol-2-yl)pyridineHCID 57503313—

Reaction Steps

Glyoxal (40% w/w H2O, 20 mL) and ammonium hydroxide (con. 40 mL) are added to a solution of 6-chloro-pyridine-2-carbaldehyde (0.127 mol; prepared from 2-chloro-6-methyl-pyridine essentially as described by Vacher et al. (1998) J. Med. Chem. 41:5080) in MeOH (620 mL) at 0° C. The mixture is allowed to warm gradually to room temperature over an 18 hour period. The solvent is removed. Water (125 mL) is added to the residue and the mixture is extracted with methylene chloride (5×150 mL). The combined organic layers are washed with brine (2×100 mL), dried and solvent removed. The crude product is triturated with ethyl ether (200 mL) to give 2-chloro-6-(1H-imidazol-2-yl)-pyridine as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07271170B2
Source datasetuspto-grants-2007_09
ORD IDord-9aa026ce563b4603986456ee72cd8715
Source noteuspto-grants-2007_09