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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705275Generated: October 25, 2026

1,2-Dichloroethane → tert-butyl (1R,2S,3S,5R)-2-azido-5-(3-(6-(2,6-difluorophenyl)-5-fluoropicolinamido)pyridin-4-yl)-3-methylcyclohexylcarbamate

https://huagongshe.com/reaction/705275

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantHOAtHCID 181649—
Reactant6-(2,6-Difluorophenyl)-5-fluoropicolinic acidHCID 59226552—
Reactanttert-butyl (1R,2S,3S,5R)-5-(3-aminopyridin-4-yl)-2-azido-3-methylcyclohexylcarbamateHCID 86705236—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Producttert-butyl (1R,2S,3S,5R)-2-azido-5-(3-(6-(2,6-difluorophenyl)-5-fluoropicolinamido)pyridin-4-yl)-3-methylcyclohexylcarbamateHCID 8670523859%

Reaction Steps

EDC (2.0 equiv.) and HOAt (2.0 equiv.) was added to a solution of tert-butyl (1R,2S,3S,5R)-5-(3-aminopyridin-4-yl)-2-azido-3-methylcyclohexylcarbamate (1.0 equiv.) and 6-(2,6-difluorophenyl)-5-fluoropicolinic acid (1.5 equiv.) in DMF (0.08 M). The mixture was stirred at ambient temperature overnight. The reaction mixture was diluted with water and extracted with ethyl acetate. The combined extracts were washed sequentially with 1M aqueous sodium hydroxide and brine, dried over sodium sulfate, filtered, concentrated and purified by ISCO SiO2 chromatography to yield tert-butyl (1R,2S,3S,5R)-2-azido-5-(3-(6-(2,6-difluorophenyl)-5-fluoropicolinamido)pyridin-4-yl)-3-methylcyclohexylcarbamate 59% yield. LC/MS (m/z)=582.3 (MH+), Rt=0.97 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09173883B2
Source datasetuspto-grants-2015_11
ORD IDord-57d0555d66834fc6a9cef0237146d75e
Source noteuspto-grants-2015_11