反应详情

温度

60 °C

A solution of 4-(3-acetoxy-4-methylanilino)-7-hydroxy-6-methoxyquinazoline hydrochloride (400 mg, 1.06 mmol), (prepared as described for the starting material in Example 1), 4-chloromethyl-2-methylthiazole hydrochloride (390 mg, 2.12 mmol), potassium carbonate (438 mg) and potassium iodide (40 mg) in DMF (15 ml) was heated at 60° C. for 15 hours. After cooling to ambient temperature the reaction mixture was partitioned between ethyl acetate and water. The organic layer was washed with brine, dried (MgSO4) and evaporated. The residue was diluted with methanol (10 ml) and 2M sodium hydroxide (2 ml) was added. After stirring for 1 hour, the reaction mixture was diluted with water (20 ml) and 2M hydrochloric acid (3 ml) was added. The resulting solid was filtered off, washed with water and dried under vacuum to give 4-(3-hydroxy-4-methylanilino)-6-methoxy-7-(2-methylthiazol-4-ylmethoxy) quinazoline hydrochloride (300 mg, 59%). m.p. 243-245° C. 1H NMR Spectrum: (DMSOd6) 2.17(s, 3H); 2.7(s, 3H); 4.0(s, 3H); 5.35(s, 2H); 7.0(dd, 1H); 7.12(d, 1H); 7.16(d, 1H); 7.58(s, 1H); 7.75(s, 1H); 8.3(s, 1H); 8.8(s, 1H); 9.5-9.8(br s, 1H); 11.3(s, 1H) MS−ESI: 409 [MH]+

1. temperatureAfter cooling to ambient temperature the reaction mixture
2. customwas partitioned between ethyl acetate and water
3. washThe organic layer was washed with brine
4. dry with materialdried (MgSO4)
5. customevaporated
6. additionThe residue was diluted with methanol (10 ml) and 2M sodium hydroxide (2 ml)
7. additionwas added
8. additionthe reaction mixture was diluted with water (20 ml) and 2M hydrochloric acid (3 ml)
9. additionwas added
10. filtrationThe resulting solid was filtered off
11. washwashed with water
12. customdried under vacuum