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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092272Generated: October 31, 2026

Trifluoroacetic acid → HCID 66590273, compound

https://huagongshe.com/reaction/1092272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-DimethylaminopyridineHCID 21885—
Reactantn-Heptyl isocyanateHCID 138341—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 66591177HCID 66591177—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 66590273HCID 6659027351.5%

Reaction Steps

300 mg (0.78 mmol) of ethyl 3-{4-[6-(tert-butoxycarbonylmethylamino)pyrid-2-yl]phenyl}acrylate are dissolved in 5 mL of dichloromethane. 2 mL of trifluoroacetic acid are added. The reaction mixture is stirred for 3 hours at room temperature. The reaction is stopped by adding 30 mL of saturated sodium hydrogen carbonate solution and is then extracted with ethyl acetate. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off and the oil obtained is then dissolved in 5 ml of dichloromethane in the presence of 1 ml of triethylamine. 630 μL (3.9 mmol, 5 eq) of heptyl isocyanate are added along with 100 mg of dimethylaminopyridine. The reaction mixture is stirred for 16 hours at reflux. The reaction is stopped by adding 30 mL of water and is then extracted with ethyl acetate. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off and the residue is then chromatographed on silica gel (80/20 to 70/30 heptane/ethyl acetate). 170 mg of ethyl 3-{4-[6-(3-heptyl-1-methylureido)pyrid-2-yl]phenyl}acrylate are obtained. Yield=51%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129416B2
Source datasetuspto-grants-2012_03
ORD IDord-88636da57f9d4b78933dec60515a560c
Source noteuspto-grants-2012_03