HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905683Generated: October 30, 2026
Benzenamine, 4-(4-morpholinyl)- → HCID 9801356, compound
https://huagongshe.com/reaction/905683
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenamine, 4-(4-morpholinyl)- | HCID 75655 | — |
| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Reactant | HCID 23071595 | HCID 23071595 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 9801356 | HCID 9801356 | 42.9% |
Reaction Steps
A 5 ml NMP solution of 352 mg of 4-morpholinoaniline was mixed with 0.95 ml of 4 M hydrogen chloride/1,4-dioxane solution and 400 mg of 4-benzylamino-2-chloropyrimidine-5-carboxamide, followed by stirring at 90° C. for 3 hours. The reaction mixture was cooled down to room temperature, and then the precipitate was collected by filtration. The collected solid was mixed with saturated sodium bicarbonate aqueous solution and extracted with a mixed solution of THF-ethyl acetate. The organic layer was washed with saturated brine, and then the solvent was evaporated. The resulting residue was crystallized by adding methanol and then recrystallized (methanol-THF) to obtain 264 mg of 4-benzylamino-2-{[4-(morpholin-4-yl)phenyl]amino}pyrimidine-5-carboxamide as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08012959B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-fd778acb8a9b42eeb93c4d9d8cac6552 |
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| Source note | uspto-grants-2011_09 |
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