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2-Amino-3-cyanopyridine-5-boronic Acid Pinacol Ester

2-Amino-3-cyanopyridine-5-boronic Acid Pinacol Ester ??? ???
?? ??:
1246372-66-6
???:
2-Amino-3-cyanopyridine-5-boronic Acid Pinacol Ester
???(??):
2-amino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinonitrile;2-amino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-3-carbonitrile;2-Amino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinecarbonitrile;3-Pyridinecarbonitrile, 2-amino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
CBNumber:
CB62538385
???:
C12H16BN3O2
??? ??:
245.09
MOL ??:
1246372-66-6.mol

2-Amino-3-cyanopyridine-5-boronic Acid Pinacol Ester ??

?? ??
Keep in dark place,Inert atmosphere,Room temperature
??
White to light brown Solid
InChI
InChI=1S/C12H16BN3O2/c1-11(2)12(3,4)18-13(17-11)9-5-8(6-14)10(15)16-7-9/h5,7H,1-4H3,(H2,15,16)
InChIKey
KRNXYPYYVHFVQS-UHFFFAOYSA-N
SMILES
C1(N)=NC=C(B2OC(C)(C)C(C)(C)O2)C=C1C#N

??

HS ?? 2933399990

2-Amino-3-cyanopyridine-5-boronic Acid Pinacol Ester C??? ??, ??, ??

Synthesis

2-amino-5-bromonicotinonitrile (50 g, 0.224 mol), bis (pinacolato) diboron (85.6 g, 0.337 mol), KOAc (44.1 g, 0.449 mol) and Pd (dppf) Cl2. CH2C12 (2.77 g, 3.4 mmol) was charged into a flask. Dioxane (400 mL) was added. The reaction mixture was stirred at 100 ℃ for 2 h under Ar. When LC-MS indicated that the reaction was completed, the mixture was cooled to room temperature. Subsequently, the mixture was filtered through diatomite, concentrated, diluted with a mixture of ethyl acetate and hexane (3:1, 1000 mL), filtered through silica gel (300-400 mesh), concentrated, crystallized and dried to give 2-Amino-3-cyanopyridine-5-boronic Acid Pinacol Ester (32 g, 66%) as a white solid.
2-Amino-3-cyanopyridine-5-boronic Acid Pinacol Ester

2-Amino-3-cyanopyridine-5-boronic Acid Pinacol Ester ?? ?? ? ???

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2-Amino-3-cyanopyridine-5-boronic Acid Pinacol Ester ?? ??

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