2-ACETYLAMINO-5-BROMOPYRIDINE
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
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)
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
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
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2-ACETYLAMINO-5-BROMOPYRIDINE(7169-97-3)Related Product Information
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- SALOR-INT L140813-1EA
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