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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183779Generated: October 30, 2026

Ethyl cyanoacetate → Ethyl 2-cyano-3-oxo-3-(2-{[3-(trifluoromethyl)phenyl]amino}-3-pyridinyl)propanoate

https://huagongshe.com/reaction/2183779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
ReactantSodium hydrideHCID 24758—
Reactant4-Nitrophenyl 2-{[3-(trifluoromethyl)phenyl]amino}nicotinateHCID 21948157—
SolventTolueneHCID 1140—
ProductEthyl 2-cyano-3-oxo-3-(2-{[3-(trifluoromethyl)phenyl]amino}-3-pyridinyl)propanoateHCID 21948193—

Reaction Steps

To a stirred mixture of NaH (524 mg, 21.8 mmol) in toluene (20 mL) was added dropwise ethyl cyanoacetate (3.7 g, 32.7 mmol, 3.5 mL). The slurry was stirred for 1 h and then 4-nitrophenyl 2-{[3-(trifluoromethyl)phenyl]amino}nicotinate (4.4 g, 10.9 mmol) was added. The reaction mixture was stirred for 1 h and then quenched with water (20 mL). CH2Cl2 (30 mL) was added and the layers were partitioned. The organic layer was washed with brine (2×) and dried over Na2SO4. The solvent was removed in vacuo and the residue was purified by silica gel flash chromatography (5:1 to 2:1 Hex:EtOAc) to afford 3 Ethyl 2-cyano-3-oxo-3-(2-{[3-(trifluoromethyl)phenyl]amino}-3-pyridinyl)propanoate. (6 g, 87%): LCMS RT: 2.83 min, MH+: 378.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900205B2
Source datasetuspto-grants-2005_05
ORD IDord-b2dd20e05c8341fab2a7c5d3e397d4e4
Source noteuspto-grants-2005_05