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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079526Generated: October 31, 2026

Dichloromethane → 6-Chloro-1-methyl-1H-imidazo[4,5-c]pyridine-4-carbonitrile

https://huagongshe.com/reaction/2079526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant3-Amino-6-chloro-4-methylamino-pyridine-2-carbonitrileHCID 57657571—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
SolventEthyl orthoformateHCID 31214—
Product6-Chloro-1-methyl-1H-imidazo[4,5-c]pyridine-4-carbonitrileHCID 57657534—

Reaction Conditions

Temperature150 °C

Reaction Steps

The suspension of 3-amino-6-chloro-4-methylamino-pyridine-2-carbonitrile (1.8 g) in DCM (5 ml), acetic acid (1.5 ml) and triethyl orthoformate (10 ml) was heated in microwave at 150° C. for 30 minutes. The mixture was then diluted with ethyl acetate (200 ml), washed with 10% sodium carbonate (100 ml), dried over sodium sulphate, solvent removed under reduced pressure, DCM (5 ml) was then added to the residue, some product crashed out and collected by filtration (0.5 g), the rest was then columned on silica gel using ethyl acetate-heptane (55:45) as eluant to give another 0.8 g expected product (a total of 1.3 g product).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932251B2
Source datasetuspto-grants-2011_04
ORD IDord-9cb56772444849cc84a05a4b26c7e5b7
Source noteuspto-grants-2011_04