反应详情

温度

90 °C

In an argon purged sealed pressure vessel was added 4-(4-chlorophenyl)-N-(4-(7-methoxy-1,5-naphthyridin-4-yloxy)phenyl)phthalazin-1-amine (0.120 g, 0.237 mmol), cesium carbonate (0.201 g, 0.617 mmol), X-phos (0.017 g, 0.0356 mmol), dichloropalladium bisacetonitrile (0.003 mg, 0.011 mmol), and acetonitrile (0.50 mL). Starting material was not soluble in acetonitrile, so added 0.5 mL 1,4 dioxane. Purged the reaction with argon, then added (triethylsilyl)acetylene (0.055 mL, 0.308 mmol), and again purged with vessel with argon, sealed, heated it to 90° C. The reaction was stirred for 1 h. Reaction complete by LC/MS. The reaction was cooled to RT, passed through pad of silica, washed with 100% CH2Cl2:MeOH(90:10)/CH2Cl2 and the organics were concentrated. The crude material was purified by silica gel chromatography eluting with 0-100% CH2Cl2:MeOH(90:10)/CH2Cl2. The product fractions were concentrated to yield N-(4-(7-methoxy-1,5-naphthyridin-4-yloxy)phenyl)-4-(4-(2-(triethylsilyl)ethynyl)phenyl)phthalazin-1-amine as light yellow solid. MS [M+H]=610.2; Calc'd 609.8 for C37H35N5O2Si.

1. customIn an argon purged
2. customsealed pressure vessel
3. customPurged
4. customthe reaction with argon
5. customsealed
6. customReaction complete by LC/MS
7. temperatureThe reaction was cooled to RT
8. washwashed with 100% CH2Cl2:MeOH(90:10)/CH2Cl2
9. concentrationthe organics were concentrated
10. customThe crude material was purified by silica gel chromatography
11. washeluting with 0-100% CH2Cl2:MeOH(90:10)/CH2Cl2
12. concentrationThe product fractions were concentrated