반응 #68562
ord-48e4ac7d27ae422c99ad679a6ab05836
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후처리
- 1기타was sparged with argon for 5 min
- 2기타Reaction
- 3온도cooled
- 4기타then partitioned between 9:1 CHCl3/IPA (20 mL) and 1M NaOH (15 mL)
- 5추출Aqueous further extracted with 9:1 CHCl3/IPA (2×10 mL)
- 6건조The combined organics dried over MgSO4
- 7농축concentrated
- 8기타purified on 40 g silica eluting with an isocratic 7% 2M NH3 in MeOH/DCM
- 9세척Product further purified prep HPLC eluting with water/ACN (0.1% TFA)
- 10기타After collected fractions
- 11workup.DISSOLUTIONwas dissolved in 1:1 ACN/water
- 12기타Resulting solid
- 13기타collected by filteration and solid
- 14세척washed with water (2 mL)
실험 절차
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.