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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407937Generated: October 29, 2026

Diisopropylethylamine → 1'-(5-Ethylpyrimidin-2-yl)-3-(2-fluoro-4-(methylsulfonyl)phenylamino)-1,4'-bipiperidin-2-one

https://huagongshe.com/reaction/407937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloro-5-ethylpyrimidineHCID 3572763—
Reactant3-(2-Fluoro-4-(methylsulfonyl)phenylamino)-1,4'-bipiperidin-2-oneHCID 67470626—
SolventDimethylformamideHCID 6228—
Product1'-(5-Ethylpyrimidin-2-yl)-3-(2-fluoro-4-(methylsulfonyl)phenylamino)-1,4'-bipiperidin-2-oneHCID 7616617751.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

3-(2-Fluoro-4-(methylsulfonyl)phenylamino)-1,4′-bipiperidin-2-one (0.300 g, 0.812 mmol), 2-chloro-5-ethylpyrimidine (0.116 g, 0.812 mmol) and DIEA (0.210 g, 1.62 mmol) were dissolved in DMF (5 mL) and heated at 100° C. overnight. The reaction was concentrated and purified over silica gel (50-100% EtOAc in hexanes) to provide 1′-(5-ethylpyrimidin-2-yl)-3-(2-fluoro-4-(methylsulfonyl)phenylamino)-1,4′-bipiperidin-2-one (0.198 g, 0.416 mmol, 51.3% yield) as white solid. Mass spectrum (apci) m/z=476.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754226B2
Source datasetuspto-grants-2014_06
ORD IDord-466b6a8e2db34dc0bdca2e0937520ee5
Source noteuspto-grants-2014_06