Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | O-Xylene | HCID 7237 | — |
| Edukt | Binap, (A+-)- | HCID 634876 | — |
| Edukt | N-(3-bromo-4-methyl-phenyl)4-(4-methyl-piperazin-1-ylmethyl)-benzamide | HCID 10309714 | — |
| Edukt | 4-(Pyridin-3-yl)pyrimidin-2-amine | HCID 12450582 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Imatinib | HCID 5291 | — |
Reaktionsschritte
To a mixture of 4-(3-pyridyl)-2-pyrimidine-amine (172.2 mg, 1.0 mmol), N-(3-bromo-4-methyl-phenyl)-4-(4-methyl-piperazin-1-ylmethyl)-benzamide (402.4 mg, 1.0 mmol) and sodium tert.-butylate (144.2 mg, 1.5 mmol) is added a mixture of rac-BINAP (31.2 mg, 0.050 mmol) and Pd2(dba)3*CHCl3 (13 mg, 0.013 mmol) under argon. After addition of 3 ml of xylene the suspension is sonicated for 10 minutes then stirred for 5 hours under reflux. After cooling to room temperature, water (10 ml) is added to the dark brown oil and the product extracted 4 times with methylene chloride (10 ml each). The combined organic extracts are dried over MgSO4 and concentrated in vacuo. The brown oil is purified by flash-chromatography (SiO2, methanol). The product, a pale yellow solid is dissolved in methylene chloride, filtered and concentrated in vacuo. Yield: 484.3 mg of the title compound, 72% of theory, (99.9% area by HPLC). The product contains typically roughly 10% of isomers which can be eliminated by preparative reversed phase chromatography.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07816359B2 |
|---|
| Quelldatensatz | uspto-grants-2010_10 |
|---|
| ORD ID | ord-214efff2b2f54554ba7e8db81d7bc8d6 |
|---|
| Quellennotiz | uspto-grants-2010_10 |
|---|