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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226336Generated: October 27, 2026

Water → ethyl (2E)-3-{6-[(1-{[(4-chlorophenyl)amino]carbonyl}-4-piperidyl)amino]-3-pyridyl}acrylate

https://huagongshe.com/reaction/226336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Chlorophenyl IsocyanateHCID 7693—
ReactantTriethylamineHCID 8471—
Reactantethyl (2E)-3-[6-(4-piperidylamino)-3-pyridyl]acrylate dihydrochlorideHCID 86603643—
SolventDimethylformamideHCID 6228—
Productethyl (2E)-3-{6-[(1-{[(4-chlorophenyl)amino]carbonyl}-4-piperidyl)amino]-3-pyridyl}acrylateHCID 8660364889.8%

Reaction Conditions

Temperature23 °C

Reaction Steps

To an ice-cooled solution of ethyl (2E)-3-[6-(4-piperidylamino)-3-pyridyl]acrylate dihydrochloride (309 mg) and Et3N (0.448 ml) In DMF (3 ml) was added 1-chloro-4-isocyanatobenzene (136 mg), the mixture was stirred at 23° C. for 1 hour. The mixed solution was poured into water (20 ml). The precipitate was collected, washed with hexane and water, dried under reduced pressure to give ethyl (2E)-3-{6-[(1-{[(4-chlorophenyl)amino]carbonyl}-4-piperidyl)amino]-3-pyridyl}acrylate (341 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557127B2
Source datasetuspto-grants-2009_07
ORD IDord-d550b8ffe5de4186addf840b3a070f75
Source noteuspto-grants-2009_07