ChemicalBook > CAS DataBase List > 2-Aminopyridine-5-boronic acid, pinacol ester

2-Aminopyridine-5-boronic acid, pinacol ester

Product Name
2-Aminopyridine-5-boronic acid, pinacol ester
CAS No.
827614-64-2
Chemical Name
2-Aminopyridine-5-boronic acid, pinacol ester
Synonyms
5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine;2-Aminopyridine-5-boronic acid;2-dioxaborolan-2-yl)pyridin-2-aMine;6-AMINOPYRIDINE-3-BORONIC ACID PINACOL ESTER;2-AMINOPYRIDINE-5-BORONIC ACID, PINACOL ESTER;(2-Aminopyridin-5-yl)boronic acid pinacol ester;(6-AMINOPYRIDIN-3-YL)BORONIC ACID PINACOL ESTER;2-AMinopyridine-5-boronic acid pinacol ester 97%;6-Aminopyridine-3-boronic acid, pinacol ester 95%;5-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine
CBNumber
CB7133659
Molecular Formula
C11H17BN2O2
Formula Weight
220.08
MOL File
827614-64-2.mol
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2-Aminopyridine-5-boronic acid, pinacol ester Property

Melting point:
131-135 °C(lit.)
Boiling point:
146°C/0.3mm
Density 
1.09±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
form 
solid
pka
7.03±0.26(Predicted)
Appearance
Off-white to light yellow Solid
Water Solubility 
Insoluble in water.
InChI
InChI=1S/C11H17BN2O2/c1-10(2)11(3,4)16-12(15-10)8-5-6-9(13)14-7-8/h5-7H,1-4H3,(H2,13,14)
InChIKey
YFTAUNOLAHRUIE-UHFFFAOYSA-N
SMILES
C1(N)=NC=C(B2OC(C)(C)C(C)(C)O2)C=C1
CAS DataBase Reference
827614-64-2(CAS DataBase Reference)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37
WGK Germany 
3
HS Code 
2933399990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
640379
Product name
2-Aminopyridine-5-boronic acid pinacol ester
Purity
97%
Packaging
1g
Price
$46.15
Updated
2025/07/31
Sigma-Aldrich
Product number
640379
Product name
2-Aminopyridine-5-boronic acid pinacol ester
Purity
97%
Packaging
5g
Price
$123.2
Updated
2025/07/31
TCI Chemical
Product number
A3206
Product name
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine
Purity
min. 98.0 %
Packaging
1G
Price
$124
Updated
2025/07/31
TRC
Product number
A629995
Product name
2-Amino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
Packaging
2.5g
Price
$105
Updated
2021/12/16
TRC
Product number
A629995
Product name
2-Amino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
Packaging
25g
Price
$580
Updated
2021/12/16
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2-Aminopyridine-5-boronic acid, pinacol ester Chemical Properties,Usage,Production

Uses

It is an important raw material and intermediate. Substrate employed in a microwave-assisted, four-component coupling process leading to amino substituted imidazopyridines.

Uses

2-Aminopyridine-5-boronic acid, pinacol ester can be used in a microwave-assisted, four-component coupling process leading to amino substituted imidazopyridines.

Synthesis

1072-97-5

73183-34-3

827614-64-2

General procedure for the synthesis of 2-aminopyridine-5-boronic acid pinacol ester from 2-amino-5-bromopyridine and biboronic acid pinacol ester: a 5L three-necked flask was assembled with a mechanical stirrer, and 300 g of 2-amino-5-bromopyridine, 528 g of biboronic acid pinacol ester, 3 L of 1,4-dioxane, 42.4 g of [Pd(dppf)2Cl2], and 593 g of anhydrous potassium acetate were added to it. . The reaction system was displaced three times with nitrogen to remove air, followed by heating to 80 °C and stirring the reaction for 16 hours. The progress of the reaction was monitored by TLC and after confirming the completion of the reaction, it was cooled to room temperature and diafiltrated. The filter cake was washed twice with 200 mL of dichloromethane, the filtrates were combined and concentrated to dryness. To the residue, 2 L of methanol was added and stirred at 37 °C overnight. Subsequently, 200 g of activated charcoal was added, stirred at room temperature and filtered. The filtrate was concentrated to dryness to obtain an oil. To the oily substance was added 150 mL of petroleum ether and 2 L of methyl tert-butyl ether (MTBE), pulsed overnight and filtered to give 380 g of 2-aminopyridine-5-boronic acid pinacol ester in 99% yield.

References

[1] Patent: CN102786543, 2016, B. Location in patent: Paragraph 0037-0043
[2] Patent: WO2007/124345, 2007, A2. Location in patent: Page/Page column 25-26
[3] European Journal of Organic Chemistry, 2012, # 3, p. 595 - 603
[4] Patent: US2015/239885, 2015, A1. Location in patent: Paragraph 0167; 0168
[5] European Journal of Medicinal Chemistry, 2016, vol. 108, p. 154 - 165

2-Aminopyridine-5-boronic acid, pinacol ester Preparation Products And Raw materials

Raw materials

Preparation Products

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2-Aminopyridine-5-boronic acid, pinacol ester Suppliers

SIGMA-RBI
Tel
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Country
Switzerland
ProdList
6896
Advantage
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View Lastest Price from 2-Aminopyridine-5-boronic acid, pinacol ester manufacturers

Shenzhen Nexcon Pharmatechs Ltd.
Product
2-Aminopyridine-5-boronic acid, pinacol ester 827614-64-2
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
2000
Release date
2025-06-19
Shaanxi Dideu Medichem Co. Ltd
Product
2-Aminopyridine-5-boronic acid, pinacol ester 827614-64-2
Price
US $1.10/g
Min. Order
1g
Purity
99.0% min
Supply Ability
100 tons min
Release date
2021-04-30
Shaanxi Dideu Medichem Co. Ltd
Product
2-Aminopyridine-5-boronic acid, pinacol ester 827614-64-2
Min. Order
1KG
Purity
99.0% min
Supply Ability
100 tons
Release date
2021-04-15

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  • 827614-64-2
  • C11H17BN2O2
  • Boronate Esters
  • Boronic Acids and Derivatives
  • Chemical Synthesis
  • Heteroaryl Boronate Esters
  • Organometallic Reagents
  • Pyridines