Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyridine compound >  Aminopyridine >  2-Chloro-3-methylaminopyridine

2-Chloro-3-methylaminopyridine

Basic information Safety Supplier Related

2-Chloro-3-methylaminopyridine Basic information

Product Name:
2-Chloro-3-methylaminopyridine
Synonyms:
  • 2-chloro-N-Methyl-3-PyridinaMine
  • 2-CHLORO-3-METHYLAMINOPYRIDINE
  • 2-CHLORO-3-(AMINOMETHYL)PYRIDINE
  • 2-CHLORO-3-METHYLAMINOPYRIDINE,=99%
  • 2-Chloro-N-methylpyridin-3-amine
  • 2-Chloro-3-methylaminepyridine
  • 3-Pyridinamine, 2-chloro-N-methyl-
  • 2-Chloro-3-methylaminopyridine ISO 9001:2015 REACH
CAS:
40932-43-2
MF:
C6H7ClN2
MW:
142.59
EINECS:
201-525-2
Product Categories:
  • pharmacetical
  • Pyridines
Mol File:
40932-43-2.mol
More
Less

2-Chloro-3-methylaminopyridine Chemical Properties

Boiling point:
144 °C(Press: 10 Torr)
Density 
1.250±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
2.73±0.10(Predicted)
More
Less

Safety Information

HS Code 
2933399990
More
Less

2-Chloro-3-methylaminopyridine Usage And Synthesis

Synthesis

6298-19-7

74-88-4

40932-43-2

2-Chloro-3-aminopyridine (0.0465 mol) was dissolved in tetrahydrofuran (45 mL) under nitrogen protection and cooled to -78 °C. A 2.0 M solution of lithium diisopropylammonium (LDA, 0.0513 mol) was added slowly and dropwise. The reaction mixture was slowly warmed to 0 °C and stirred at this temperature for 1 hour. Subsequently, the reaction mixture was cooled again to -78 °C and iodomethane (0.0582 mol) was added. The reaction mixture was slowly warmed to room temperature and stirring was continued for 16 hours. Upon completion of the reaction, the reaction was quenched by the addition of saturated ammonium chloride solution and the mixture was extracted with ethyl acetate. The organic layers were combined, dried with anhydrous sodium sulfate, filtered and the solvent was concentrated under reduced pressure. The residue was purified by silica gel short column chromatography (eluent: hexane/ethyl acetate, 80/20). The fraction containing the target product was collected and the solvent was concentrated under reduced pressure to give 5.91 g of 2-chloro-3-methylaminopyridine (intermediate compound 1) in 89% yield.

References

[1] Patent: WO2004/106298, 2004, A1. Location in patent: Page 19-20
[2] Synthesis, 1999, # 11, p. 1893 - 1902
[3] Advanced Functional Materials, 2018, vol. 28, # 44,
[4] Patent: US2004/19051, 2004, A1. Location in patent: Page 11

2-Chloro-3-methylaminopyridineSupplier

Shanghai Sphchem Co., Ltd.
Tel
021-56491756 13512199871
Email
2819742715@qq.com
SuZhou ShiYa Biopharmaceuticals, Inc.
Tel
86(512)5235 8471 17715136450
Email
sales@shiyabiopharm.com
TIANJIN SPRING PHARMA SCIENCE CO., LTD.
Tel
0086-22-60330256
BePharm Ltd
Tel
400-685-9117
Email
market@bepharm.com
Amadis Chemical Company Limited
Tel
571-89925085
Email
sales@amadischem.com