HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 7-Bromo-4-(2-methoxy-4-(trifluoromethyl)phenyl)-2-methylquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-Bromo-4-chloro-2-methylquinazoline | HCID 22247819 | — |
| Reactant | (2-Methoxy-4-(trifluoromethyl)phenyl)boronic acid | HCID 24901776 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 7-Bromo-4-(2-methoxy-4-(trifluoromethyl)phenyl)-2-methylquinazoline | HCID 86687735 | 51.7% |
Reaction Steps
A solution of PdCl2(dppf)-CH2Cl2 adduct (0.159 g, 0.194 mmol), (2-methoxy-4-(trifluoromethyl)phenyl)boronic acid (0.940 g, 4.27 mmol), 7-bromo-4-chloro-2-methylquinazoline (ACES Pharma, 1.000 g, 3.88 mmol), and potassium carbonate (2.147 g, 15.53 mmol) in 12 mL dioxane was treated with 4 mL water and was allowed to stir overnight at room temperature. LC/MS showed mostly product, so the aqueous layer was removed, and the reaction mixture was concentrated. Purification of the crude residue by silica gel column chromatography (0-50% EtOAc/heptane) gave 7-bromo-4-(2-methoxy-4-(trifluoromethyl)phenyl)-2-methylquinazoline (0.797 g, 2.007 mmol, 51.7% yield). (M+H)+=396.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09012443B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-2cc2beaecb2a41c5b7644b8b2a313520 |
| Source note | uspto-grants-2015_04 |