反应详情

温度

100 °C

A 20 mL microwave vial was charged with 3-methyl-5-(1,3-thiazol-5-yl)aniline (500 mg, 2.63 mmol), cesium carbonate (2.99 g, 9.20 mmol), 2-chloro-4-cyclopropylpyrimidine (INTERMEDIATE 29, 406 mg, 2.63 mmol), and dioxane (10.4 mL). The system was purged and flushed with argon (3×) before adding XantPhos (228 mg, 0.394 mmol) and palladium(II) acetate (59 mg, 0.263 mmol). The system was then purged and flushed with argon (3×) before sealing and heating to 100° C. for 2 h. Upon completion the mixture was cooled to room temperature, diluted with ethyl acetate, filtered through celite washing with ethyl acetate, and concentrated under reduced pressure. Purification by column chromatography on silica gel (0-60% ethyl acetate in hexanes) provided 603 mg (1.96 mmol, 74%) of 4-cyclopropyl-N-[3-methyl-5-(1,3-thiazol-5-yl)phenyl]pyrimidin-2-amine as a yellow solid. MS ESI: [M+H]+ m/z 309.2.

1. customThe system was purged
2. customflushed with argon (3×)
3. customThe system was then purged
4. customflushed with argon (3×)
5. temperatureUpon completion the mixture was cooled to room temperature
6. additiondiluted with ethyl acetate
7. filtrationfiltered
8. washthrough celite washing with ethyl acetate
9. concentrationconcentrated under reduced pressure
10. customPurification by column chromatography on silica gel (0-60% ethyl acetate in hexanes)