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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303307Generated: October 31, 2026

Water → HCID 18460825, compound

https://huagongshe.com/reaction/2303307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 18460846HCID 18460846—
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
SolventEthyl AcetateHCID 8857—
ProductHCID 18460825HCID 18460825—

Reaction Steps

A 4 ml portion of 4 M hydrochloric acid-dioxane solution was added to 183 mg of tert-butyl ester of {4-[5-carbamoyl-4-(3-methylanilino)pyrimidin-2-ylamino]benzyl}carbamic acid, followed by stirring at room temperature for 16 hours. Water and ethyl acetate were added to the reaction mixture, the thus formed insoluble matter was removed by filtration and the filtrate was alkalified by adding 1 M sodium hydroxide aqueous solution. After extraction with ethyl acetate, the organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The residue concentrated under a reduced pressure was recrystallized from a mixed solvent of ethyl acetate and n-hexane, thereby obtaining 44 mg of 2-(4-aminomethylanilino)-4-(3-methylanilino)pyrimidine-5-carboxamide (light yellow crystals).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432963B1
Source datasetuspto-grants-2002_08
ORD IDord-50254f8cbf1e490294426cd21fcf55e3
Source noteuspto-grants-2002_08