ChemicalBook > Product Catalog >Chemical Reagents >Organic reagents >Borate >[6-[benzoyl(methyl)amino]-5-methyl-3-pyridyl]boronic acid

[6-[benzoyl(methyl)amino]-5-methyl-3-pyridyl]boronic acid

[6-[benzoyl(methyl)amino]-5-methyl-3-pyridyl]boronic acid Structure
CAS No.
446299-81-6
Chemical Name:
[6-[benzoyl(methyl)amino]-5-methyl-3-pyridyl]boronic acid
Synonyms
Ozenoxacin Impurity 7;Ozenoxacin Impurity 15;5-Methyl-6-(phenacylamino)pyridin-3-yl]boronic acid;(5-methyl-6-(N-methylbenzamido)pyridin-3-yl)boronic acid;[6-[benzoyl(methyl)amino]-5-methyl-3-pyridyl]boronic acid;[6- [benzoyl (methyl) amino] -5-methyl-3-pyridinyl] boric acid;(5-methyl-6-((2-oxo-2-phenylethyl)amino)pyridin-3-yl)boronic acid;Boronic acid, [6-(benzoylmethylamino)-5-methyl-3-pyridinyl]- (9CI);(S) - 6-chloro-3,4-dihydro-2h-thieno [3,2-e] - 1,2-thiazine-4-alcohol 1,1-dioxide;(ethyl 7-chloro-8-methyl-4-oxo-1,4-dihydroquinoline-3-carboxylate),[6-[benzoyl(methyl)amino]-5-methyl-3- pyridyl]boronic acid
CBNumber:
CB23370678
Molecular Formula:
C14H15BN2O3
Molecular Weight:
270.09
MOL File:
446299-81-6.mol
Modify Date:
2023/10/16 17:43:51

[6-[benzoyl(methyl)amino]-5-methyl-3-pyridyl]boronic acid Properties

Boiling point 513.7±60.0 °C(Predicted)
Density 1.27±0.1 g/cm3(Predicted)
vapor pressure 0Pa at 25℃
pka 4.12±0.18(Predicted)
form Solid:particulate/powder
LogP 2.87

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS09
Signal word  Warning
Hazard statements  H317-H411
Precautionary statements  P261-P272-P280-P302+P352-P333+P313-P321-P363-P501

[6-[benzoyl(methyl)amino]-5-methyl-3-pyridyl]boronic acid Chemical Properties,Uses,Production

Uses

[6-[benzoyl(methyl)amino]-5-methyl-3-pyridyl]boronic acid can be used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process.

Synthesis

Synthesis_446299-81-6
Under a nitrogen atmosphere, N-(5-bromo-3-methyl-2-pyridinyl)-N-methylbenzamide 30.0 g was dissolved in 150 mL of tetrahydrofuran, triisopropyl borate 22.0 g was added. The reaction mixture was colled to-60 .DEGREE CELSIUS., n-butyl lithium (1.56 mol/L n-hexane solution) 69 mL was added dropwise required to between 20 minutes, and the mixture was stirred for 15 minutes at the same temperature.After raising the temperature of the reaction mixture at-20 .DEGREE CELSIUS., 390 mL of water was added dropwise, it was stirred for 30 min at room temperature,the aqueous layer was separated. The aqueous layer was fractionated and HCl 1 mol/L was added to adjust the pH at 4.5,the precipitate was collected by filtration, 6-[benzoyl(methyl)amino]-5-methyl-3-pyridinylboric acid 18.5 g was obtained as colorless solid.

[6-[benzoyl(methyl)amino]-5-methyl-3-pyridyl]boronic acid Preparation Products And Raw materials

Raw materials

Preparation Products

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Ozenoxacin Impurity 7 (S) - 6-chloro-3,4-dihydro-2h-thieno [3,2-e] - 1,2-thiazine-4-alcohol 1,1-dioxide (ethyl 7-chloro-8-methyl-4-oxo-1,4-dihydroquinoline-3-carboxylate),[6-[benzoyl(methyl)amino]-5-methyl-3- pyridyl]boronic acid [6- [benzoyl (methyl) amino] -5-methyl-3-pyridinyl] boric acid Boronic acid, [6-(benzoylmethylamino)-5-methyl-3-pyridinyl]- (9CI) 5-Methyl-6-(phenacylamino)pyridin-3-yl]boronic acid [6-[benzoyl(methyl)amino]-5-methyl-3-pyridyl]boronic acid (5-methyl-6-(N-methylbenzamido)pyridin-3-yl)boronic acid Ozenoxacin Impurity 15 (5-methyl-6-((2-oxo-2-phenylethyl)amino)pyridin-3-yl)boronic acid 446299-81-6 C14H15BN2O3 446299-81-6