Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyridine compound >  Bromopyridine >  2-ACETYLAMINO-5-BROMOPYRIDINE

2-ACETYLAMINO-5-BROMOPYRIDINE

Basic information Safety Supplier Related

2-ACETYLAMINO-5-BROMOPYRIDINE Basic information

Product Name:
2-ACETYLAMINO-5-BROMOPYRIDINE
Synonyms:
  • N-ACETYLAMINO-5-BROMOPYRIDINE
  • N-(5-BROMO-PYRIDIN-2-YL)-ACETAMIDE
  • 2-ACETYLAMINO-5-BROMOPYRIDINE, PURISS, 98%
  • 2-ACETAMIDO-5-BROMOPYRIDINE
  • 2-ACETYLAMINO-5-BROMOPYRIDINE
  • Acetamide, N-(5-bromo-2-pyridinyl)-
  • JR-8242, 2-Acetylamino-5-bromopyridine, 97%
  • 2-Acetamido-5-bromopyridine >
CAS:
7169-97-3
MF:
C7H7BrN2O
MW:
215.05
EINECS:
626-709-0
Product Categories:
  • pharmacetical
  • Pyridine
  • C8 to C9
  • Carbonyl Compounds
  • Esters
  • C7 and C8Heterocyclic Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Pyridines
Mol File:
7169-97-3.mol
More
Less

2-ACETYLAMINO-5-BROMOPYRIDINE Chemical Properties

Melting point:
175-179 °C (lit.)
Boiling point:
372.2±27.0 °C(Predicted)
Density 
1.630±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
powder to crystal
pka
12.94±0.70(Predicted)
color 
White to Light yellow
CAS DataBase Reference
7169-97-3(CAS DataBase Reference)
More
Less

Safety Information

Hazard Codes 
Xn,T
Risk Statements 
22-36/37/38-43-40
Safety Statements 
26-36/37/39-22
WGK Germany 
3
HS Code 
29339900
More
Less

2-ACETYLAMINO-5-BROMOPYRIDINE Usage And Synthesis

Chemical Properties

White powder

Uses

2-Acetamido-5-bromopyridine is a chemical reagent used in the synthesis of novel Bcr-Abl inhibitors with diacylated piperazine felxible linkers. Also used to produce hetero-monocyclic derivatives as even more potent inhibitors of BCR-ABL.

Synthesis

1072-97-5

108-24-7

7169-97-3

2-Amino-5-bromopyridine (86.50 g, 500 mmol), acetic anhydride (153 g, 1500 mmol) and 850 mL of acetic acid were added to a 2000 mL single-necked round-bottomed flask with a magnetic stirrer turned on. The reaction mixture was stirred at 100 °C for 9 hours. After confirming the complete reaction of 2-amino-5-bromopyridine by thin layer chromatography (TLC) and gas chromatography (GC) monitoring, water was added to the reaction solution. Subsequently, the reaction was filtrated and the filter cake was washed with a solvent mixture of ethyl acetate and n-hexane (1:4, v/v) to obtain the pure product 2-acetamido-5-bromopyridine. The filtrate was extracted with ethyl acetate, and the extract was concentrated by rotary evaporation to obtain the crude product, which was recrystallized with a mixed solvent of ethyl acetate and hexane (1:4, v/v) and further purified to obtain 2-acetamido-5-bromopyridine. The product was dried and the calculated yield was 75.40%, and the purity was 99.68% as determined by high performance liquid chromatography (HPLC).

References

[1] Patent: CN103601745, 2017, B. Location in patent: Paragraph 0029; 0030
[2] Tetrahedron Letters, 2002, vol. 43, # 17, p. 3121 - 3123
[3] Patent: WO2011/130628, 2011, A1. Location in patent: Page/Page column 205
[4] Patent: US2013/102595, 2013, A1. Location in patent: Paragraph 0480; 0481
[5] Patent: JP2015/187145, 2015, A. Location in patent: Paragraph 0414

2-ACETYLAMINO-5-BROMOPYRIDINESupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
INTATRADE GmbH
Tel
+49 3493/605464
Email
sales@intatrade.de
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Email
Sales-CN@TCIchemicals.com