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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(4-Methylpiperazin-1-yl)aniline | HCID 737253 | — |
| Reactant | Alumina | HCID 9989226 | — |
| Reactant | HCID 10705897 | HCID 10705897 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 5330252 | HCID 5330252 | 50% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06498163B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-72691a4b9e324c0ea359630455c24e3b |
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| Source note | uspto-grants-2002_12 |
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