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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875439Generated: October 28, 2026

Pyridine → Ethyl{[(2-fluorophenyl)acetyl]amino}(pyridin-2-yl)acetate

https://huagongshe.com/reaction/1875439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantEthyl 2-amino-2-(pyridin-2-yl)acetateHCID 4570669—
Reactant2-(2-Fluorophenyl)acetyl chlorideHCID 14004011—
SolventEthyl AcetateHCID 8857—
ProductEthyl{[(2-fluorophenyl)acetyl]amino}(pyridin-2-yl)acetateHCID 59177860—

Reaction Conditions

Temperature0 °C

Reaction Steps

2.50 g (12.1 mmol) of ethyl amino(pyridin-2-yl)acetate [G. van Zyl et al., J. Org. Chem. 1961, 26, 3373] are introduced into 20 ml of dichloromethane and, after addition of 4.9 ml (60.3 mmol) of pyridine, cooled to 0° C. A solution of 1.86 g (12.1 mmol) of (2-fluorophenyl)acetyl chloride is then slowly added, and the mixture is stirred at 0° C. for 30 min and then at RT for 2 h. It is diluted with ethyl acetate, washed with sodium bicarbonate solution and dried over sodium sulfate. The crude product is purified by chromatography on silica gel (eluent: cyclohexane/ethyl acetate 1:1). 2.9 g (76% of theory) of the desired product are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309551B2
Source datasetuspto-grants-2012_11
ORD IDord-44e0f0e40f9942dda44ef6d4750baa38
Source noteuspto-grants-2012_11