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CAS No. : | 1036991-24-8 | MDL No. : | MFCD11975406 |
Formula : | C13H21BN2O2 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | KSAMKARQFVLMFC-UHFFFAOYSA-N |
M.W : | 248.13 | Pubchem ID : | 51072189 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P280-P305+P351+P338 | UN#: | |
Hazard Statements: | H302-H315-H319-H332-H335 | Packing Group: | |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
76% | With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate; In 1,4-dioxane; at 100℃; for 12h;Inert atmosphere; | To a solution of 5-bromo-2-(NN-dimethylamino)pyridine (8.5 g, 42.3 mmol) and 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1,3,2-dioxaborolane) (12.9 g, 50.7 mmol) in dioxane (10 mL) was added KOAc (8.3 g, 84.6 mmol) and Pd(dppf)Cl2 (1.55 g, 2.1 mmol) at 25 C under N2. The mixture was heated to 100 C and stirred at this temperature for 12 hours. LCMS showed that the reaction was complete. The mixture was filtered and concentrated under reduced pressure to give a residue which was purified by silica gel column chromatography (petroleum ether / ethyl acetate=50/1 to 3/1) to give 2-(2-(N,N-dimethylamino)pyrid-5-yl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (8 g, 32.2 mmol, 76% yield) as a yellow solid 1H NMR 400 MHz CDCl3 = 8.53 (s, 1H), 7.75-7.78 (d, 1H), 6.43-6.45 (d, 1H), 3.09 (s, 6H), 1.22-1.30 (m, 12H). ESI-MS (m/z): 249.2 (M+H)+ |
With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate; In 1,4-dioxane; at 20℃;Inert atmosphere; | PdCI2(dppf)-CH2Cl2 adduct (81 mg, 0.099 mmol) was added to a solution of 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2-dioxaborolane) (379 mg, 1 .492 mmol), 5-bromo- N,N-dimethylpyridin-2-amine (200 mg, 0.995 mmol) and potassium acetate (293 mg, 2.98 mmol) in 1 ,4-dioxane (40 mL) at room temperature under an atmosphere of nitrogen. The resulting solution was stirred at 100 C for 12 hr. The system was filtered and the filtrate was concentrated to afford crude product.which was used for the next step. LCMS: [M+H] 249.1 . |
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