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(2-AMINO-4-PYRIDYL)BORONIC ACID

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Products Intro: Product Name:(2-AMINO-4-PYRIDYL)BORONIC ACID
CAS:903513-62-2
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Products Intro: Product Name:(2-AMINO-4-PYRIDYL)BORONIC ACID
CAS:903513-62-2
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CAS:903513-62-2
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Products Intro: Product Name:(2-aminopyridin-4-yl)boronic acid
CAS:903513-62-2
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Products Intro: Product Name:(2-Aminopyridin-4-yl)boronicaci
CAS:903513-62-2

(2-AMINO-4-PYRIDYL)BORONIC ACID manufacturers

(2-AMINO-4-PYRIDYL)BORONIC ACID Basic information
Product Name:(2-AMINO-4-PYRIDYL)BORONIC ACID
Synonyms:(2-AMINO-4-PYRIDYL)BORONIC ACID;2-aminopyridin-4-ylboronic acid;2-Aminopyridine-4-boronic acid;2-aMino-4-pyridinyl boronic acid;(2-Aminopyridin-4-yl);Boronic acid, B-(2-amino-4-pyridinyl)-;(2-Aminopyridin-4-yl)boronicaci;(2-AMINO-4-PYRIDYL)BORONIC ACID ISO 9001:2015 REACH
CAS:903513-62-2
MF:C5H7BN2O2
MW:137.93
EINECS:1533716-785-6
Product Categories:6
Mol File:903513-62-2.mol
(2-AMINO-4-PYRIDYL)BORONIC ACID Structure
(2-AMINO-4-PYRIDYL)BORONIC ACID Chemical Properties
Boiling point 411.7±55.0 °C(Predicted)
density 1.33±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Store in freezer, under -20°C
pka5.74±0.10(Predicted)
AppearanceOff-white to gray Solid
Safety Information
MSDS Information
(2-AMINO-4-PYRIDYL)BORONIC ACID Usage And Synthesis
Synthesis
2-Amino-4-chloropyridine

19798-80-2

(2-AMINO-4-PYRIDYL)BORONIC ACID

903513-62-2

General procedure for the synthesis of (2-aminopyridin-4-yl)boronic acid from 2-amino-4-chloropyridine: 2-amino-4-chloropyridine (3 g, 23.34 mmol), bis(pinacolato)diboron (17.78 g, 70.1 mmol), 2-dicyclohexylphosphino-2',6'-dimethoxybiphenyl (0.38 g, 0.93 mmol), tris( dibenzylideneacetone) dipalladium(0) (0.21 g, 0.23 mmol) and potassium acetate (3.89 g, 39.67 mmol) were mixed in 1,4-dioxane (78 mL) under nitrogen atmosphere. The reaction mixture was stirred at 100 °C for 3 hours. Upon completion of the reaction, the hot reaction mixture was filtered through diatomaceous earth and washed with ethyl acetate (EtOAc). The organic layer was concentrated under vacuum and the residue was precipitated with diisopropyl ether (DIPE) to afford the intermediate compound 1-24 ((2-aminopyridin-4-yl)boronic acid) as a white solid (5.84 g, quantitative yield), which could be used in the next reaction without further purification.

References[1] Patent: WO2014/195311, 2014, A1. Location in patent: Page/Page column 88
[2] Bioorganic and Medicinal Chemistry Letters, 2009, vol. 19, # 7, p. 1879 - 1882
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