CAS 286961-14-6: N-Boc-1,2,5,6-tetrahydropyridine-4-boronic acid pinacol ester
Description:N-Boc-1,2,5,6-tetrahydropyridine-4-boronic acid pinacol ester is a chemical compound characterized by its unique structure, which includes a tetrahydropyridine ring, a boronic acid moiety, and a pinacol ester. The "N-Boc" designation indicates the presence of a tert-butyloxycarbonyl (Boc) protecting group on the nitrogen atom, which is commonly used in organic synthesis to protect amines. This compound is typically utilized in medicinal chemistry and organic synthesis due to its ability to participate in various reactions, including Suzuki coupling, which is essential for forming carbon-carbon bonds. The boronic acid functionality allows for the formation of stable complexes with diols, while the pinacol ester enhances its stability and solubility in organic solvents. Additionally, the tetrahydropyridine structure contributes to its potential biological activity, making it a valuable intermediate in the development of pharmaceuticals. Overall, N-Boc-1,2,5,6-tetrahydropyridine-4-boronic acid pinacol ester is a versatile compound with significant applications in synthetic organic chemistry.
Formula:C16H28BNO4
InChI:InChI=1/C16H28BNO4/c1-14(2,3)20-13(19)18-10-8-12(9-11-18)17-21-15(4,5)16(6,7)22-17/h8H,9-11H2,1-7H3
- Synonyms:
- 3,6-Dihydro-2H-pyridine-1-tert-butoxycarbonyl-4-boronic acid pinacol ester
- N-Boc-1,2,5,6-tetrahydropyridine-4-(pinacolato)boronate
- tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine-1-carboxylate
- tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate
- 3,6-Dihydro-2H-pyridine-1-N-Boc-4-boronic acid pinacol ester
- Tert-Butyl 5,6-Dihydro-4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyridine-1(2H)-Carboxylate
- 4-(4,4,5,5-Tetramethyl-[1,3,2]Dioxaborolan-2-Yl)-3,6-Dihydro-2H-Pyridine-1-Carboxylic Acid Tert-Butyl Ester
- Tert-Butyl 4-(Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-1,2,3,6-Tetrahydropyridine-1-Carboxylate
