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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1423341Generated: October 26, 2026

4-Methylmorpholine → 4-(4-cyclopropyl-1H-imidazol-1-yl)picolinic acid

https://huagongshe.com/reaction/1423341

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant4-Fluoropyridine-2-carboxylic acidHCID 18327805—
ReactantAcetonitrile methanolHCID 21959252—
ReactantHCID 178420870HCID 178420870—
SolventHydrochloric AcidHCID 313—
SolventDimethylformamideHCID 6228—
Product4-(4-cyclopropyl-1H-imidazol-1-yl)picolinic acidHCID 5803565079.9%

Reaction Conditions

Temperature35 °C

Reaction Steps

A mixture of 4-fluoropicolinic acid (400 mg, 2.84 mmol) and 4-cyclopropyl-1H-imidazole (322 mg, 2.98 mmol) were dissolved in N,N-dimethylformamide, and N-methylmorpholine (0.36 ml, 3.28 mmol) was added. The reaction was warmed to 35° C., and stirred for 20 hours. The solvent was then removed under reduced pressure to afford a viscous oily residue. This residue was dissolved in 1N hydrochloric acid (5 mL), and the aqueous layer was extracted with ethyl acetate (2×5 mL). The aqueous layer was concentrated under reduced pressure to afford a yellow solid. To this residue was added 5 mL of acetonitrile/methanol (20:1) and the mixture was sonicated to afford a fine suspension of solids. The solids were collected by filtration, washed several times with acetonitrile, and dried on the filter funnel. The yellow solids were collected to afford 520 mg (69% yield) of 4-(4-cyclopropyl-1H-imidazol-1-yl)picolinic acid as the hydrochloride salt. M+1=230.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927582B2
Source datasetuspto-grants-2015_01
ORD IDord-d199db2781874f89a06bff4bcce8474a
Source noteuspto-grants-2015_01