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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717487Generated: November 2, 2026

Triethylamine → 5-(Azidomethyl)pyridine-2-carbonitrile

https://huagongshe.com/reaction/1717487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium AzideHCID 33557—
ReactantMethanesulfonateHCID 85257—
Reactant2-Cyano-5-hydroxymethylpyridineHCID 12251966—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product5-(Azidomethyl)pyridine-2-carbonitrileHCID 2190462783%

Reaction Steps

5-(Hydroxymethyl)pyridine-2-carbonitrile (4 g, 0.03 mol; see step (ii) above) was dissolved in 25 mL of methylene chloride and cooled in an ice bath. Mesyl chloride (2.32 mL, 0.0300 mol) and then triethylamine (4.6 mL, 0.033 mol) were added dropwise. The reaction mixture was stirred and after work up the crude mesylate was treated with NaN3 (7.35 g, 0.113 mol) in 20 mL of DMF. The reaction mixture was stirred at 40° C. for 2 h, diluted with water and extracted with ethyl acetate. The organic layer was concentrated to yield 3.95 g (83%) of the crude azide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803954B2
Source datasetuspto-grants-2010_09
ORD IDord-8da2d29cb6d149c197384b4c650166ee
Source noteuspto-grants-2010_09