Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718335Generated: October 29, 2026

Diisopropylethylamine → Ethyl 2-(5-bromo-4-(4,4-dimethylpiperidin-1-yl)-2,6-dimethylpyridin-3-yl)-2-oxoacetate

https://huagongshe.com/reaction/718335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4,4-DimethylpiperidineHCID 138100—
ReactantEthyl 2-(5-bromo-4-chloro-2,6-dimethylpyridin-3-yl)-2-oxoacetateHCID 118307784—
SolventAcetonitrileHCID 6342—
ProductEthyl 2-(5-bromo-4-(4,4-dimethylpiperidin-1-yl)-2,6-dimethylpyridin-3-yl)-2-oxoacetateHCID 11830778971.6%

Reaction Steps

To a solution of 4,4-dimethylpiperidine (1.245 g, 11.00 mmol) and DIEA (3.49 ml, 20.00 mmol) in anhydrous CH3CN (40 mL) was added ethyl 2-(5-bromo-4-chloro-2,6-dimethylpyridin-3-yl)-2-oxoacetate (3.21 g, 10 mmol) at rt. The resulting mixture was placed in a pre-heated oil bath (80° C.). After 22 h, the reaction mixture was concentrated and the residue was purified by flash chromatography using 1-lit each 2.5, 5, 7.5 and 10% EtOAc/Hex to afford ethyl 2-(5-bromo-4-(4,4-dimethylpiperidin-1-yl)-2,6-dimethylpyridin-3-yl)-2-oxoacetate (2.846 g, 7.16 mmol, 71.6% yield) as yellow solid. 1H NMR (500 MHz, CDCl3) δ 4.37 (q, J=7.1 Hz, 2H), 3.67-2.75 (br.s., 4H), 2.71 (s, 3H), 2.44 (s, 3H), 1.42 (t, J=7.1 Hz, 3H), 1.38 (t, J=5.6 Hz, 4H), 1.00 (s, 6H). LCMS (M+H)=399.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193720B2
Source datasetuspto-grants-2015_11
ORD IDord-ccda779be53d40069e7b15f35a6f6161
Source noteuspto-grants-2015_11