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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 562915Generated: October 25, 2026

Ethyl Acetate → Methyl 2-(4-azepan-1-yl-3-cyanophenyl)isonicotinate

https://huagongshe.com/reaction/562915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantMethyl 2-(3-cyano-4-fluorophenyl)isonicotinateHCID 66995083—
SolventDimethyl SulfoxideHCID 679—
ProductMethyl 2-(4-azepan-1-yl-3-cyanophenyl)isonicotinateHCID 66995069—

Reaction Conditions

Temperature50 °C

Reaction Steps

In 7 ml of DMSO was dissolved 2.22 g of methyl 2-(3-cyano-4-fluorophenyl)isonicotinate, and 2.44 ml of hexamethyleneimine was added thereto, followed by heating at 50° C. for 5 hours. After cooling, the reaction solution was diluted with ethyl acetate and was washed with 1M hydrochloric acid, a saturated aqueous sodium hydrogen carbonate solution, and brine, successively. The organic layer was dried and then concentrated under reduced pressure and the resulting residue was dissolved in a mixed solvent of ethyl acetate and diisopropyl ether. Activated carbon was added thereto, followed by stirring for 1 hour. Then, the activated carbon was removed by filtration and washed with ethyl acetate. The resulting filtrate and washing liquid were combined and concentrated to obtain 2.58 g of methyl 2-(4-azepan-1-yl-3-cyanophenyl)isonicotinate. (2) Then, 2.49 g of the compound was dissolved in a mixed solvent of 15 ml of methanol and 30 ml of THF, and 11 ml of a 1M aqueous sodium hydroxide solution was added thereto, followed by heating at 80° C. for 1 hour.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067446B2
Source datasetuspto-grants-2011_11
ORD IDord-639eace32c3a47839a011c2662d7fe62
Source noteuspto-grants-2011_11