Basic information Safety Supplier Related

4-PHENYL-PYRIDIN-2-YLAMINE

Basic information Safety Supplier Related

4-PHENYL-PYRIDIN-2-YLAMINE Basic information

Product Name:
4-PHENYL-PYRIDIN-2-YLAMINE
Synonyms:
  • 4-PHENYL-PYRIDIN-2-YLAMINE
  • 2-AMINO-4-PHENYLPYRIDINE
  • 4-phenyl-2-pyridinamin
  • 4-phenylpyridin-2-amine
  • 4-phenyl-
  • 4-phenyl-2-aminopyridine
  • 4-Phenyl-2-pyridinamine
  • 4-Phenylpyridine-2-amine
CAS:
60781-83-1
MF:
C11H10N2
MW:
170.21
Product Categories:
  • API intermediates
Mol File:
60781-83-1.mol
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4-PHENYL-PYRIDIN-2-YLAMINE Chemical Properties

Melting point:
164-165 °C(Solv: benzene (71-43-2))
Boiling point:
343.7±30.0 °C(Predicted)
Density 
1.133±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
form 
solid
pka
6.63±0.11(Predicted)
color 
Yellow
EPA Substance Registry System
2-Amino-4-phenylpyridine (60781-83-1)
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Safety Information

Risk Statements 
41
Safety Statements 
26-39
HS Code 
2933399990
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4-PHENYL-PYRIDIN-2-YLAMINE Usage And Synthesis

Synthesis Reference(s)

Journal of Medicinal Chemistry, 21, p. 874, 1978 DOI: 10.1021/jm00207a007
The Journal of Organic Chemistry, 72, p. 4554, 2007 DOI: 10.1021/jo070189y

Synthesis

84249-14-9

98-80-6

60781-83-1

General procedure for the synthesis of 2-amino-4-phenylpyridine from 2-amino-4-bromopyridine and phenylboronic acid: phenylboronic acid (141 mg, 1.156 mmol), 4-bromo-2-amino-pyridine (200 mg, 1.156 mmol) and PdCl2(dppf)-CH2Cl2 adduct (94 mg, 0.116 mmol) were suspended in a mixture of 1,2 -dimethoxyethane (3 mL) and 1 M aqueous sodium carbonate (3.47 mL, 3.47 mmol) in a mixed solvent. The reaction mixture was stirred at 90 °C for 5 h and subsequently cooled to room temperature. The reaction mixture was filtered through a diatomaceous earth pad and the filter cake was washed with dichloromethane (DCM). The filtrate was concentrated under reduced pressure to remove the solvent, and the resulting crude product was purified by silica gel column chromatography (Biotage 40M column) using 0-10% methanol/dichloromethane gradient elution to afford the target product 2-amino-4-phenylpyridine (195 mg, 1.146 mmol, 99% yield). The product structure was confirmed by 1H NMR (400 MHz, CDCl3) and UPLC-MS: 1H NMR δ 4.49 (dd, 2H), 6.69-6.78 (m, 1H), 6.90 (dd, 1H), 7.39-7.52 (m, 3H), 7.56-7.68 (m, 2H), 8.10-8.17 (m, 1H); UPLC-MS: tR = 0.42 min, m/z = 171 [M + H]+.

References

[1] Patent: US2009/203705, 2009, A1. Location in patent: Page/Page column 49
[2] Journal of Medicinal Chemistry, 2016, vol. 59, # 24, p. 11171 - 11181
[3] Patent: WO2017/141036, 2017, A1. Location in patent: Page/Page column 50

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