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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269844Generated: October 31, 2026

P-Anisidine → HCID 67388964, compound

https://huagongshe.com/reaction/269844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantSodium BicarbonateHCID 516892—
ReactantPotassium FluorideHCID 522689—
Reactant4-(Benzylamino)-2-(methanesulfonyl)pyrimidine-5-carboxamideHCID 23071581—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 67388964HCID 6738896424%

Reaction Conditions

Temperature95 °C

Reaction Steps

A 5 ml portion of NMP solution containing 300 mg of 4-benzylamino-2-(methylsulfonyl)pyrimidine-5-carboxamide was mixed with 122 mg of p-anisidine and 58 mg of potassium fluoride, followed by stirring at 90 to 100° C. for 21 hours. During this period, 58 mg of potassium fluoride was added three times. The reaction mixture was cooled down to room temperature, diluted with water, mixed with saturated sodium bicarbonate aqueous solution and then extracted with ethyl acetate. The organic layer was washed with saturated brine, and then the solvent was evaporated. The resulting residue was purified by a silica gel column chromatography (chloroform:methanol) and then recrystallized (methanol-THF) to obtain 82 mg of 4-benzylamino-2-[(4-methoxyphenyl)amino]pyrimidine-5-carboxamide as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449456B2
Source datasetuspto-grants-2008_11
ORD IDord-5e6f16be713442e3825606d281106d69
Source noteuspto-grants-2008_11