反应详情

温度

100 °C

A suspension of 1-(2-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethanol (228 mg, 807 μmol), N-((6-chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)-7-methoxy-1,5-naphthyridin-4-amine (197 mg, 576 μmol), dichloro[1,1′bis(diphenylphoshino)ferrocene]palladium(ii)dichloromethane adduct (127 mg, 173 μmol), cesium carbonate (751 mg, 2306 μmol) in dioxane (3 mL) and water (0.6 mL) was sparged with argon for 5 min then heated to 100° C. for 6 h. Reaction cooled then partitioned between 9:1 CHCl3/IPA (20 mL) and 1M NaOH (15 mL). Aqueous further extracted with 9:1 CHCl3/IPA (2×10 mL). The combined organics dried over MgSO4. concentrated, then purified on 40 g silica eluting with an isocratic 7% 2M NH3 in MeOH/DCM. Product further purified prep HPLC eluting with water/ACN (0.1% TFA). After collected fractions were reduced to a clear the residue was dissolved in 1:1 ACN/water and pH adjusted to 9 with 1M NaOH (3-4 drops). Resulting solid collected by filteration and solid washed with water (2 mL). MS (ESI pos. ion) m/z: 462 (MH+). Calc'd exact mass for C23H20ClN7O2: 461.

1. customwas sparged with argon for 5 min
2. customReaction
3. temperaturecooled
4. customthen partitioned between 9:1 CHCl3/IPA (20 mL) and 1M NaOH (15 mL)
5. extractionAqueous further extracted with 9:1 CHCl3/IPA (2×10 mL)
6. dry with materialThe combined organics dried over MgSO4
7. concentrationconcentrated
8. custompurified on 40 g silica eluting with an isocratic 7% 2M NH3 in MeOH/DCM
9. washProduct further purified prep HPLC eluting with water/ACN (0.1% TFA)
10. customAfter collected fractions
11. dissolutionwas dissolved in 1:1 ACN/water
12. customResulting solid
13. customcollected by filteration and solid
14. washwashed with water (2 mL)