8-bromo-5-fluoroquinoline

8-bromo-5-fluoroquinoline Suppliers list
Company Name: Energy Chemical  
Tel: 400-0056266
Email: sales8178@energy-chemical.com
Company Name: Wuhan Chemwish Technology Co., Ltd  
Tel: 86-027-67849912
Email: sales@chemwish.com
Company Name: ZEROSCHEM.CO.,LTD.  
Tel: 10-61256048 13810278579;
Email: sales@zeroschem.com
Company Name: Shandong Xiya Chemical Co., Ltd  
Tel: 13355009207 13355009207
Email: 3007715519@qq.com
Company Name: Chengdu Forest Science and Technology Development Co., Ltd.  
Tel: 18030648795 18030648795
Email: sales@cdforestchem.com

8-bromo-5-fluoroquinoline manufacturers

8-bromo-5-fluoroquinoline Basic information
Uses
Product Name:8-bromo-5-fluoroquinoline
Synonyms:8-bromo-5-fluoroquinoline;Quinoline, 8-bromo-5-fluoro-
CAS:917251-99-1
MF:C9H5BrFN
MW:226.05
EINECS:
Product Categories:
Mol File:917251-99-1.mol
8-bromo-5-fluoroquinoline Structure
8-bromo-5-fluoroquinoline Chemical Properties
Boiling point 294.2±20.0 °C(Predicted)
density 1.647±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka1.35±0.29(Predicted)
AppearanceWhite to off-white Solid
Safety Information
HS Code 2933491090
MSDS Information
8-bromo-5-fluoroquinoline Usage And Synthesis
Uses8-Bromo-5-fluoroquinoline is used as a novel binder in the synthesis of 5HT1A, and also acts as a receptor antagonist and agonist. This drug has excellent efficacy for central nervous system disorders, such as cognitive impairment, anxiety disorders, depression, and sexual dysfunction.
Synthesis
2-Bromo-5-fluoroaniline

1003-99-2

Glycerol

56-81-5

8-bromo-5-fluoroquinoline

917251-99-1

2-Bromo-5-fluoroaniline (100 g, 1.0 eq.), 4-nitrophenol (40 g, 0.54 eq.) and glycerol (97 g, 2.0 eq.) were slowly added to pre-mixed sulfuric acid (267 mL) and water (114 mL) at 140-150 °C and the reaction lasted for 1.5 h. The reaction was carried out by HPLC. At the beginning of the reaction, the relative area percentage of 4-nitrophenol was shown to be 37.8% by HPLC analysis. The content of 4-nitrophenol decreased to 4.7% after the addition of 50% of the feedstock and further decreased to 5.0% after the addition of all the feedstock. Upon completion of the reaction, 8-bromo-5-fluoroquinoline was obtained after post-treatment in 87.5% yield with 0.29% total impurities. In addition, reducing the amount of 4-nitrophenol to 0.46 equivalents (34 g) was also successful in synthesizing the target intermediate in acceptable yield.

References[1] Patent: US2007/27160, 2007, A1. Location in patent: Page/Page column 66
[2] Patent: US2007/299083, 2007, A1. Location in patent: Page/Page column 9
[3] Patent: WO2007/146072, 2007, A2. Location in patent: Page/Page column 73-74
[4] Patent: WO2008/67390, 2008, A2. Location in patent: Page/Page column 101-102
[5] Patent: US2007/27160, 2007, A1. Location in patent: Page/Page column 63-65
8-bromo-5-fluoroquinoline Preparation Products And Raw materials
Raw materials2-Bromo-5-fluoroaniline-->4-Nitrophenol-->Sulfuric acid-->Glycerol
Tag:8-bromo-5-fluoroquinoline(917251-99-1) Related Product Information
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