Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 3-(4-Methylpiperazin-1-yl)aniline | HCID 11564613 | — |
| Reactant | HCID 57974155 | HCID 57974155 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57974201 | HCID 57974201 | — |
Reaction Steps
Ethyl 2-[(2-chloro-5-fluoro-4-pyrimidinyl)amino]benzoate (1.0 g, 3.4 mmol), 3-(4-methyl-1-piperazinyl)aniline (0.65 g, 3.4 mmol), ethanol (45 mL) and 6N HCl (1.5 mL, 8.8 mmol) were heated with stirring in a reaction vessel, which was sealed and heated at 95° C. for 24 h. The reaction mixture was cooled to room temperature, poured into water, extracted with ethyl acetate and neutralized to pH 7 by the slow addition of 6N NaOH. The resulting precipitate was collected on a sintered glass funnel and washed with water and ethyl ether to afford the title compound as a tan solid; yield 1.0 g (65%). MS: M(C24H27FN6O2)=450.52 (M+H)+=451.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07884098B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-49219537b7a94f6b978467b2d2869914 |
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| Source note | uspto-grants-2011_02 |
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