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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300063Generated: November 1, 2026

4-(4-Methylpiperazin-1-yl)aniline → HCID 5330252, compound

https://huagongshe.com/reaction/2300063

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Methylpiperazin-1-yl)anilineHCID 737253—
ReactantAluminaHCID 9989226—
ReactantHCID 10705897HCID 10705897—
SolventChloroformHCID 6212—
ProductHCID 5330252HCID 533025250%

Reaction Conditions

Temperature175 °C

Reaction Steps

To 8-isopropyl-2-methanesulfinyl-8H-pyrido[2,3-d]pyrimidin-7-one (212 mg, 0.85 mmol) was added 4-(4-methylpiperazin-1-yl)-aniline (323 mg, 1.69 mmol). The reaction mixture was heated at 175° C. for 10 minutes then cooled to room temperature and partitioned between saturated sodium bicarbonate and chloroform. The organic layer was washed with brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified by flash chromatography eluting with 10% methanol in ethyl acetate. The fractions containing product were concentrated, and hexane and ethyl acetate were added to give a solid that was dissolved in chloroform and passed through an aluminum oxide column. The fractions containing product were concentrated, and upon addition of hexane and ethyl acetate, a solid formed providing 160 mg (50%) of 8-isopropyl-2-[4-(4-methylpiperazin-1-yl)-phenylamino]-8H-pyrido[2,3-d]pyrimidin-7-one, mp 221-222° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498163B1
Source datasetuspto-grants-2002_12
ORD IDord-72691a4b9e324c0ea359630455c24e3b
Source noteuspto-grants-2002_12