Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 988974Generated: October 30, 2026

Ethyl Acetate → HCID 22250895, compound

https://huagongshe.com/reaction/988974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium AzideHCID 33557—
ReactantHCID 22250915HCID 22250915—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 22250895HCID 22250895—

Reaction Conditions

Temperature100 °C

Reaction Steps

6-Chloro-N-[2-(2,4-dichlorophenyl)ethyl]pyridine-3-carboxamide (1 equivalent) and sodium azide (2.6 equivalents) were suspended in anhydrous DMSO (0.6 M) under nitrogen. The mixture was heated at 100° C. for four days. Ethyl acetate was added and the organic phase washed with water and brine, dried over anhydrous sodium sulfate, and filtered. The filtrate was evaporated to dryness and the resultant residue dissolved in a 1:1 ethyl acetate/DCM mixture. This solution was purified by flash chromatography over silica (1:1 ethyl acetate/DCM). The fractions coeluting with the major band (Rf 0.53, eluent: 1:1 ethyl acetate/DCM) were combined and evaporated to dryness. The residue was recrystallized from acetonitrile to give 6-azido-N-[2-(2,4-dichlorophenyl)ethyl]-pyridine-3-carboxamide as pale yellow needles. LCMS (MH+) 336.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06638927B2
Source datasetuspto-grants-2003_10
ORD IDord-f837a65a6dfd4d3b94de158fa90fa815
Source noteuspto-grants-2003_10