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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067136Generated: October 30, 2026

Potassium Carbonate → 4-(2,5-Difluoro-phenylamino)-6-[4-(3-isopropyl-[1,2,4]oxadiazol-5-yl)-piperidin-1-yl]-pyrimidine-5-carbonitrile

https://huagongshe.com/reaction/2067136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,5-DifluoroanilineHCID 67775—
Reactant4,6-Dichloropyrimidine-5-carbonitrileHCID 599371—
Reactant4-(3-(Propan-2-yl)-1,2,4-oxadiazol-5-yl)piperidineHCID 24208845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-(2,5-Difluoro-phenylamino)-6-[4-(3-isopropyl-[1,2,4]oxadiazol-5-yl)-piperidin-1-yl]-pyrimidine-5-carbonitrileHCID 58216415—

Reaction Steps

To a solution of 4,6-Dichloro-pyrimidine-5-carbonitrile (254 mg, 1.47 mmol) and 2,5-difluoroaniline (190 mg, 1.47 mmol) in DMF (3 mL) at 0° C. was added K2CO3 (203 mg, 1.47 mmol). The completion of the reaction was monitored by TLC (EtOAc:Hex=1:1, Rf=0.90). After the reaction was complete, 4-(3-isopropyl-[1,2,4]oxadiazol-5-yl)-piperidine (340 mg, 1.47 mmol) and K2CO3 (406 mg, 2.94 mmol) were added at 0° C. The reaction was warmed to rt and stirred for 30 min. The reaction was heated to 40° C. and maintained for 1 h. The reaction was cooled to rt, poured in to H2O (50 mL) and extracted with EtOAc (50 mL, two times). The EtOAc was dried over MgSO2 and concentrated under vacuum. The crude product was purified over SiO2 (EtoAc:Hex=1:1, Rf=0.44) to afford the desired Compound B131 (465 mg; 71.1%). 1H-NMR (DMSO-d6): 9.32 (1H, s), 8.19 (1H, s), 7.40˜7.08 (3H, m), 4.54 (2H, m), 3.48˜3.32 (4H, m), 3.07˜3.01 (2H, m), 2.18˜2.14 (2H, b), 1.96˜1.86 (2H, m), 1.27 (6H, d) ppm. LCMS: 426.43.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293751B2
Source datasetuspto-grants-2012_10
ORD IDord-dcbe55ad45b14f42a3a04b0c3c6d8850
Source noteuspto-grants-2012_10