Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501444Generated: October 31, 2026

Dimethylformamide → t-Butyl 4-(3-benzyl-4-chloro-3H-imidazo(4,5-c]pyridin-2-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/501444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant3-Benzyl-2,4-dichloro-1,3-dihydroimidazo[4,5-c]pyridineHCID 57472844—
SolventEthyl AcetateHCID 8857—
Productt-Butyl 4-(3-benzyl-4-chloro-3H-imidazo(4,5-c]pyridin-2-yl)piperazine-1-carboxylateHCID 2307058914.9%

Reaction Conditions

Temperature150 °C

Reaction Steps

0.094 g of t-butyl piperazine-1-carboxylate was added to a 1 ml N,N-dimethylformamide solution of 0.127 g of 3-benzyl-2,4-dichloro-1,3-dihydroimidazo[4,5-c]pyridine, and the mixture was heated at 150° C. for two hours. 25 ml of ethyl acetate was added to the mixture, and the organic layer was washed three times with 10 ml of water and then with 10 ml of an aqueous solution saturated with sodium chloride. The organic liquid was dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography. Thus, 0.029 g of the title compound was obtained from the fraction eluted with ethyl acetate-hexane (3:2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772226B2
Source datasetuspto-grants-2010_08
ORD IDord-18f80efefcc84a9fb204b98854d12c0f
Source noteuspto-grants-2010_08