HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225500Generated: November 1, 2026
Ethyl Acetate → Imatinib (Pyridine)-N-oxide
https://huagongshe.com/reaction/225500
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 68489405 | HCID 68489405 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Imatinib (Pyridine)-N-oxide | HCID 9827642 | — |
Reaction Steps
N-Methylpiperazine (99 mg, 1.0 mmol) is added to a stirred suspension of 4-chloromethyl-N-[4-methyl-3-[[4-(1-oxido-3-pyridinyl)-2-pyrimidinyl]-amino]-phenyl]-benzamide (220 mg, 0.49 mmol) In ethanol (5 mL). The mixture is then stirred at 10° C. for 15 h to give a solution, which is then cooled to RT and treated with ethyl acetate (200 mL). The resulting solution is washed with aqueous sodium hydroxide (100 mL of 2M) and saturated aqueous sodium chloride solution (100 mL), dried (Na2SO4), filtered and the solvent is evaporated off under reduced pressure to yield the crude product which is purified by column chromatography on silica gel, eluent 25% aqueous ammonia-methanol-dichloromethane (0.5:10:90) to give the title compound as a yellow crystalline solid, m.p. 232-235° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07557105B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-fb62a2f977a04b689846f3cfbaee395e |
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| Source note | uspto-grants-2009_07 |
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