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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905698Generated: October 29, 2026

Benzenamine, 4-(4-morpholinyl)- → HCID 67388756, compound

https://huagongshe.com/reaction/905698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenamine, 4-(4-morpholinyl)-HCID 75655—
ReactantSodium BicarbonateHCID 516892—
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ReactantHCID 23071569HCID 23071569—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 67388756HCID 6738875613.4%

Reaction Conditions

Temperature90 °C

Reaction Steps

A 6 ml portion of NMP solution containing 303 mg of 4-cyclohexylamino-2-(methylsulfonyl)pyrimidine-5-carboxamide was mixed with 1.05 ml of 1 M n-tetrabutylammonium fluoride/THF solution, followed by stirring at 90° C. for 1 hour. Next, this was mixed with 200 mg of 4-morpholinoaniline and 2.77 ml of 4 M hydrogen chloride/1,4-dioxane solution, followed by stirring at 90° C. for 3 hours. 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-THF mixed solution. The organic layer was washed with saturated brine, and then the solvent was evaporated and the resulting residue was purified by a silica gel column chromatography (chloroform:methanol) to obtain 54 mg of 4-cyclohexylamino-2-[(4-morpholinophenyl)amino]pyrimidine-5-carboxamide as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012959B2
Source datasetuspto-grants-2011_09
ORD IDord-7185c310b5f94f9eb8a61f2e0d7f5cd4
Source noteuspto-grants-2011_09