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4-(Bromoacetyl)pyridine hydrobromide

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Products Intro: Product Name:2-Bromo-1-(pyridin-4-yl)ethanone hydrobromide
CAS:5349-17-7
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
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Products Intro: Product Name:2-Bromo-1-(pyridin-4-yl)ethanone hydrobromide
CAS:5349-17-7
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Products Intro: Product Name:4-(Bromoacetyl)pyridinehydrobromide
CAS:5349-17-7
Purity:0.98 Package:1g;5g;25g;100;500g
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Products Intro: Product Name:4-(bromoacetyl)pyridine hydrobromide
CAS:5349-17-7
Purity:99% Package:1kg

4-(Bromoacetyl)pyridine hydrobromide manufacturers

4-(Bromoacetyl)pyridine hydrobromide Basic information
Product Name:4-(Bromoacetyl)pyridine hydrobromide
Synonyms:BUTTPARK 37\12-45;2-BROMO-1-PYRDIN-4-YLETHAN-1-ONE HYDROBROMIDE;2-BROMO-1-(4-PYRIDINYL)-1-ETHANONE HYDROBROMIDE;4-(BROMOACETYL)PYRIDINE HYDROBROMIDE;4-(2-BROMO-ACETYL)-PYRIDINIUM, BROMIDE;2-Bromo-1-pyridin-4-ylethanone hydrobromide;2-Bromo-1-pyrdin-3-ylethan-1-one hydrobromide;2-Bromo-1-(pyridin-4-yl)ethan-1-one hydrobromide
CAS:5349-17-7
MF:C7H7Br2NO
MW:280.94
EINECS:621-664-3
Product Categories:Heterocyclic Compounds;Acetyl Halides;CHIRAL CHEMICALS;Acetyl Halides;Pyridines
Mol File:5349-17-7.mol
4-(Bromoacetyl)pyridine hydrobromide Structure
4-(Bromoacetyl)pyridine hydrobromide Chemical Properties
Melting point 194 °C
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
form powder
color Off-white
Water Solubility Soluble in water.
CAS DataBase Reference5349-17-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-22
Safety Statements 26-36/37/39-37/39
Hazard Note Irritant
HazardClass 8
HS Code 2933399990
MSDS Information
4-(Bromoacetyl)pyridine hydrobromide Usage And Synthesis
UsesDesign and synthesis of potent, selective, and orally bioavailable tetrasubstituted imidazole inhibitors of p38 mitogen-activated protein kinase 4-(Bromoacetyl)pyridine hydrobromide was used to prepare 2-Phenyl-4-(4-pyridyl)imidazole.
Synthesis
4-Acetylpyridine

1122-54-9

4-(Bromoacetyl)pyridine hydrobromide

5349-17-7

General procedure for the synthesis of 4-(bromoacetyl)pyridine hydrobromide from 4-acetylpyridine: 558 g of batch master batch was added to a reaction flask, followed by the addition of 42 g of ethyl acetate, and 121.1 g of 4-acetylpyridine was added slowly with stirring, keeping the reaction temperature at 20~30 °C and stirring well. N-bromosuccinimide (NBS) 186.9 g was added in batches, followed by slow warming to 65~75 °C. The progress of the reaction was monitored by thin layer chromatography (TLC) until the feedstock was fully reacted. After completion of the reaction, the reaction mixture was cooled to 0~10°C to allow complete crystallization of the product. The crystals were collected by filtration, washed and pulped with 650 g of deionized water, filtered again, and dried to give 275.6 g of 4-(bromoacetyl)pyridine hydrobromide as a white solid in 98.1% molar yield.

References[1] Patent: WO2005/73225, 2005, A1. Location in patent: Page/Page column 49-50
[2] Patent: CN106632001, 2017, A. Location in patent: Paragraph 0026; 0027; 0028; 0029
[3] Journal of Medicinal Chemistry, 2010, vol. 53, # 2, p. 787 - 797
[4] Patent: WO2009/158393, 2009, A1. Location in patent: Page/Page column 51
[5] Patent: US2007/142415, 2007, A1. Location in patent: Page/Page column 17
4-(Bromoacetyl)pyridine hydrobromide Preparation Products And Raw materials
Raw materialsAcetic acid-->Bromine-->Hydrogen bromide-->4-Acetylpyridine-->3-Acetylpyridine-->N-Bromosuccinimide-->Ethyl acetate
Tag:4-(Bromoacetyl)pyridine hydrobromide(5349-17-7) Related Product Information
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