Basic information Safety Supplier Related

5-chloro-N-methylpyridin-2-amine

Basic information Safety Supplier Related

5-chloro-N-methylpyridin-2-amine Basic information

Product Name:
5-chloro-N-methylpyridin-2-amine
Synonyms:
  • 2-PyridinaMine, 5-chloro-N-Methyl-
  • 5-chloro-N-methylpyridin-2-amine
  • UKRORGSYN-BB BBR-009506
  • 5-Chloro-2-(MethylaMino)pyridine
  • 5-Chloro-2-MethylaMinopyridine
  • 5-Chloro-N-Methyl-2-pyridineaMine
  • 5-Chloro-N-methyl-2-pyridinamine
  • (5-Chloro-pyridin-2-yl)-methyl-amine
CAS:
4214-80-6
MF:
C6H7ClN2
MW:
142.59
Mol File:
4214-80-6.mol
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5-chloro-N-methylpyridin-2-amine Chemical Properties

Melting point:
63-65°C
Boiling point:
247℃
Density 
1.250
Flash point:
103℃
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
DMSO, Methanol
form 
Solid
pka
5.00±0.10(Predicted)
color 
Off-White
InChI
InChI=1S/C6H7ClN2/c1-8-6-3-2-5(7)4-9-6/h2-4H,1H3,(H,8,9)
InChIKey
KSISYWKRGRATSK-UHFFFAOYSA-N
SMILES
C1(NC)=NC=C(Cl)C=C1
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Safety Information

HS Code 
2933399990
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5-chloro-N-methylpyridin-2-amine Usage And Synthesis

Chemical Properties

Off-White Solid

Uses

5-Chloro-2-methylaminopyridine is used in the preparation of aminosulfuranes with N-heterocyclic groups.

Synthesis

1072-98-6

7318-81-2

4214-80-6

GENERAL METHOD: Copper(II) acetate (0.550 g, 3.03 mmol) was added to a solution of 2-amino-5-chloropyridine (1.22 mmol) and pyridine (0.34 mL, 4.24 mmol) in dioxane (15 mL). The mixture was stirred for 15 min, methylboronic acid (0.181 g, 3.03 mmol) was added and the reaction was refluxed until the 2-amino-5-chloropyridine was completely consumed (reaction time monitored by TLC analysis, 1.5-18 h). The reaction mixture was allowed to cool to room temperature, filtered through diatomaceous earth and the solvent was evaporated. The residue was purified by fast chromatography (elution gradient: 0→50% ethyl acetate/hexane) to give 5-chloro-N-methylpyridin-2-amine (162). Preparation of 5-chloro-N-methylpyridin-2-amine (162): compound 162 was prepared from 2-amino-5-chloropyridine (160) according to the above method F. 73 mg of brown powder was obtained in 42% yield. 1H NMR (500 MHz, CDCl3) δ 2.90 (s, 3H), 4.79 (br s, 1H), 6.33 (d, J = 8.9 Hz, 1H), 7.38 (dd, J = 2.6, 8.9 Hz, 1H), 8.02 (d, J = 2.6 Hz, 1H). 13C NMR (126 MHz, CDCl3) δ 29.22, 106.90, 119.44, 137.27, 146.26, 157.88. LC-MS (M + H+) calculated value C6H7ClN2 143, measured value 143.

References

[1] Patent: WO2014/100833, 2014, A1. Location in patent: Paragraph 0081; 0233

5-chloro-N-methylpyridin-2-amineSupplier

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