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2-Amino-3-bromo-5-fluoropyridine

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Products Intro: Product Name:2-Amino-3-bromo-5-fluoropyridine
CAS:869557-43-7
Purity:98%(Min,GC) Package:1G;1KG;100KG
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Products Intro: Product Name:3-bromo-5-fluoropyridin-2-amine
CAS:869557-43-7
Purity:0.99 Package:5G,10G,25G,50G,100G,250G,1KG
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CAS:869557-43-7
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Products Intro: Product Name:2-Amino-3-bromo-5-fluoropyridine
CAS:869557-43-7
Purity:98% Package:100g, 500g, 1kg, 25kg, 50kg, 200kg Remarks:API intermediate
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Products Intro: CAS:869557-43-7
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2-Amino-3-bromo-5-fluoropyridine manufacturers

2-Amino-3-bromo-5-fluoropyridine Basic information
Product Name:2-Amino-3-bromo-5-fluoropyridine
Synonyms:3-Bromo-5-fluoropyridin-2-amine;2-AMINO-3-BROMO-5-FLUOROPYRIDINE;2-AMINO-5-FLUORO-3-BROMO PYRIDINE;3-BroMo-5-fluoro-pyridin-2-ylaMine;2-Amino-3-bromo-5-fluoropyridine 97%;2-Pyridinamine, 3-bromo-5-fluoro-;2-Amino-3-bromo-5-fL;2-Amino-3-bromo-5-fluoropyridine ISO 9001:2015 REACH
CAS:869557-43-7
MF:C5H4BrFN2
MW:191
EINECS:
Product Categories:Fluorine series;Building Blocks;C5;C5 to C6;Chemical Synthesis;Fluorinated Building Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks;Heterocyclic Fluorinated Building Blocks;Other Fluorinated Heterocycles;Boronic Acid;Amines;blocks;FluoroCompounds;Pyridines
Mol File:869557-43-7.mol
2-Amino-3-bromo-5-fluoropyridine Structure
2-Amino-3-bromo-5-fluoropyridine Chemical Properties
Melting point 61-63°C
Boiling point 63-65℃
density 1.813±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
form powder to crystal
pka1.86±0.49(Predicted)
color White to Almost white
CAS DataBase Reference869557-43-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 22-37/38-41
Safety Statements 26-39
WGK Germany 3
HS Code 29333990
MSDS Information
2-Amino-3-bromo-5-fluoropyridine Usage And Synthesis
Uses2-Amino-3-bromo-5-fluoropyridine is a reactant used in the synthesis of cyano heteroaryl bromides.
Synthesis
2-Amino-5-fluoropyridine

21717-96-4

2-Amino-3-bromo-5-fluoropyridine

869557-43-7

The general procedure for the synthesis of 2-amino-3-bromo-5-fluoropyridine from 2-amino-5-fluoropyridine is as follows: Method C: Bromination reaction using sulfuric acid (H2SO4). This was done as follows: a solution of 93% sulfuric acid (12.5 kg, 119 mol) in water (26 L) was added to a 50 L reactor, followed by 2-amino-5-fluoropyridine (6.5 kg, 58 mol). The reaction temperature was adjusted to 30 °C and then bromine (10 kg, 63 mol) was added in 10 portions over 3 hours. The reaction mixture was stirred at 45 °C for 18 hours, followed by continued stirring at 50 °C for 5 hours. Upon completion of the reaction, the mixture was cooled to 15 °C and transferred to a 400 L reactor for post-processing. The products of the four reactions (4 x 6.5 kg) were combined and the reaction was quenched with a mixture of 50% sodium hydroxide (110 kg, 1375 mol) and sodium thiosulfate (1.8 kg, 11.4 mol) in water (100 L) at 50 °C, the quenching process lasted for 1-3 hours. The temperature was adjusted to 32 °C, the slurry was filtered and washed with water (80 L) to give a water-wet crude product (62 kg). The same operation was carried out for the second round of three reactions (3 x 6.5 kg of feedstock) to give a water-wet crude product (41 kg). The crude product (103 kg) was dissolved (partially insoluble) in toluene (280 kg) at 25-30 °C. After addition of brine (20 kg), phase separation could not be achieved due to the presence of solids. The mixture was filtered through a diatomaceous earth pad, washed with toluene and layered. The organic phase was concentrated to 347 L to remove residual water by azeotropy and used in the subsequent preparation of compound 3a. The product concentration was determined by aliquoting to be 181 g/L in a yield of 62.8 kg. An additional 600 g of product was obtained by extraction of the water/brine layer by ethyl acetate (10 L) and separated, which was treated by filtration through a pad of magnesium salts, evaporation, and hexane grinding. The overall yield was 82%.

References[1] Patent: WO2015/73481, 2015, A1. Location in patent: Paragraph 0259-0260
[2] Patent: WO2016/183116, 2016, A1. Location in patent: Paragraph 0251; 0252; 0253
[3] Patent: WO2017/97234, 2017, A1. Location in patent: Paragraph 00405
[4] Patent: WO2011/143366, 2011, A1. Location in patent: Page/Page column 75
[5] Patent: WO2011/143365, 2011, A1. Location in patent: Page/Page column 154
2-Amino-3-bromo-5-fluoropyridine Preparation Products And Raw materials
Raw materials2-Amino-5-fluoropyridine-->Sulfuric acid
Preparation Products1H-Pyrrolo[2,3-b]pyridine, 4-broMo-2-cyclopropyl-5-fluoro--->8-Bromo-6-fluoro-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine
Tag:2-Amino-3-bromo-5-fluoropyridine(869557-43-7) Related Product Information
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