تفاعل #68611
ord-3c483852cdbc403497b1e754dee62bb0
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىflushed with argon
- 2أخرىsealed
- 3أخرىplaced in a 100° C.
- 4أخرىfor 5 hours
- 5تركيزThe reaction mixture was concentrated
- 6workup.ADDITIONdiluted with DCM and chloroform
- 7غسيلThis was washed with water, sat. NaHCO3, and brine
- 8تجفيفdried with MgSO4
- 9ترشيحfiltered
- 10تركيزconcentrated
- 11أخرىto give a brown oil
- 12أخرىThis was purified by HPLC
الإجراء التجريبي
A 48 mL tube was charged with sodium 2-chloro-2,2-difluoroacetate (0.15 g, 1.0 mmol), 4-((6-(3-methylisoxazol-5-yl)-[1,2,4]triazolo[4,3-a]pyridin-3-yl)methoxy)quinolin-7-ol hydrobromide (0.200 g, 0.44 mmol), cesium carbonate (0.43 g, 1.3 mmol), and DMF (1.7 ml, 22 mmol), flushed with argon, sealed, then placed in a 100° C. oil bath for 5 hours. The reaction mixture was concentrated, then diluted with DCM and chloroform. This was washed with water, sat. NaHCO3, and brine, then dried with MgSO4, filtered, and concentrated to give a brown oil. This was purified by HPLC to give 7-(difluoromethoxy)-4-((6-(3-methylisoxazol-5-yl)-[1,2,4]triazolo[4,3-a]pyridin-3-yl)methoxy)quinoline (0.025 g, 13% yield) as the formic acid salt. MS (ESI pos. ion) m/z: 424 (MH+). Calc'd exact mass for C21H15F2N5O3: 423.