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579525-46-5

579525-46-5 Structure

579525-46-5 Structure
IdentificationBack Directory
[Name]

2-(Dimethylamino)pyridine-5-boronic acid hydrate
[CAS]

579525-46-5
[Synonyms]

2-DiMethylaMino-5-pyridineboronic acid
2-(Dimethylamino)pyridine-5-boronicacid
5-Borono-2-(dimethylamino)pyridine hydrate
2-(Dimethylamino)pyridine-5-boronic acid 97%
Boronic acid, B-[6-(dimethylamino)-3-pyridinyl]-
2-(DIMETHYLAMINO)PYRIDINE-5-BORONIC ACID HYDRATE
6-(DIMETHYLAMINO)PYRIDINE-3-BORONIC ACID HYDRATE
Boronic acid, [6-(dimethylamino)-3-pyridinyl]- (9CI)
2-(N,N-Dimethylamino)pyridine-5-boronic acid hydrate
2-(Dimethylamino)pyridine-5-boronic acid hydrate ISO 9001:2015 REACH
[Molecular Formula]

C7H11BN2O2
[MDL Number]

MFCD06656059
[MOL File]

579525-46-5.mol
[Molecular Weight]

165.99
Chemical PropertiesBack Directory
[Boiling point ]

352.3±52.0 °C(Predicted)
[density ]

1.19±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Store in freezer, under -20°C
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

4.21±0.10(Predicted)
[color ]

Yellow
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H335-H302-H319-H332-H315
[Precautionary statements ]

P261-P271-P304+P340-P312-P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

22
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
Hazard InformationBack Directory
[Uses]

2-(Dimethylamino)pyridine-5-boronic acid, hydrade
[Synthesis]

5-Bromo-2-(dimethylamino)pyridine

26163-07-5

Bis(pinacolato)diboron

73183-34-3

2-(Dimethylamino)pyridine-5-boronic acid hydrate

579525-46-5

General procedure for the synthesis of 2-(dimethylamino)pyridine-5-boronic acid from 5-bromo-N,N-dimethylpyridin-2-amine and pinacol ester of bis(boronic acid): to a solution of 1,4-dioxane (20 mL) in 5-bromo-N,N-dimethylpyridin-2-amine (400 mg, 1.989 mmol), was added sequentially 4,4,4',4',5,5,5',5'-octa methyl-2,2'-bis(1,3,2-dioxaborolane) (606 mg, 2.387 mmol), PdCl2(dppf)-CH2Cl2 adduct (162 mg, 0.199 mmol) and potassium acetate (390 mg, 3.98 mmol). The reaction mixture was heated to 100 °C and stirred overnight under nitrogen protection. After completion of the reaction, the mixture was filtered and the filtrate was concentrated under vacuum to afford the crude product (6-(dimethylamino)pyridin-3-yl)boronic acid (420 mg, 0.496 mmol, 25% yield) as a brown oil.LCMS analysis showed the [M+H]+ peak at 167.1.

[References]

[1] Patent: WO2017/98440, 2017, A1. Location in patent: Page/Page column 170
Spectrum DetailBack Directory
[Spectrum Detail]

2-(Dimethylamino)pyridine-5-boronic acid hydrate(579525-46-5)1HNMR
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