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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295987Generated: October 30, 2026

Dimethylcarbamoyl Chloride → 3-(Azidomethyl)-6-methyl-2-pyridinecarbonitrile

https://huagongshe.com/reaction/1295987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylcarbamoyl ChlorideHCID 6598—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22929836HCID 22929836—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product3-(Azidomethyl)-6-methyl-2-pyridinecarbonitrileHCID 2292980677.4%

Reaction Steps

Trimethylsilyl cyanide (6.4 ml, 48 mmol) and dimethylcarbamyl chloride (4.2 ml, 46 mmol) were added in that order to a solution of the 5-(azidomethyl)-2-methyl-1-pyridiniumolate (7.08 g, 43.2 mmol) in methylene chloride (80 ml) at room temperature and the mixture was stirred at the same temperature for 23 hours. After confirming completion of the reaction by thin layer chromatography, saturated aqueous sodium hydrogencarbonate (80 ml) was added and the mixture was stirred for 10 minutes. The reaction mixture was diluted with ethyl acetate, the aqueous layer was separated and extraction was performed with ethyl acetate. The collected organic layer was washed with water and brine and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the residue was purified by silica gel column chromatography (solvent: n-hexane-ethyl acetate) to yield the title compound (5.79 g, 56%, two steps) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244730B2
Source datasetuspto-grants-2007_07
ORD IDord-10e015eea24c4a74b5f0c1ecba813f20
Source noteuspto-grants-2007_07