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FLOSEQUINAN

Product Name
FLOSEQUINAN
CAS No.
76568-02-0
Chemical Name
FLOSEQUINAN
Synonyms
Manoplax;BTS-49465;Flosequinon;FLOSEQUINAN;FLOSEQUINAN USP/EP/BP;7-Huom-1-methyl-3-(methylsulfinyl)-4(1H)-quinolinone;7-Fluoro-1-methyl-3-methylsulfinylquinolin-4(1H)-one;7-Fluoro-1-methyl-3-(methylsulfinyl)-4(1H)-quinolinone;4(1H)-Quinolinone, 7-fluoro-1-methyl-3-(methylsulfinyl)-
CBNumber
CB9292729
Molecular Formula
C11H10FNO2S
Formula Weight
239.27
MOL File
76568-02-0.mol
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FLOSEQUINAN Property

Melting point:
226-228°
Boiling point:
423.1±45.0 °C(Predicted)
Density 
1.44±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
pka
-0.51±0.70(Predicted)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
API0003253
Product name
FLOSEQUINAN
Purity
95.00%
Packaging
1MG
Price
$749
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0003253
Product name
FLOSEQUINAN
Purity
95.00%
Packaging
5MG
Price
$776
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0003253
Product name
FLOSEQUINAN
Purity
95.00%
Packaging
10MG
Price
$806
Updated
2021/12/16
AHH
Product number
MT-51803
Product name
Flosequinan
Purity
98%
Packaging
0.5g
Price
$910
Updated
2021/12/16
Chemenu
Product number
CM144014
Product name
7-fluoro-1-methyl-3-(methylsulfinyl)quinolin-4(1H)-one
Purity
95%
Packaging
1g
Price
$1866
Updated
2021/12/16
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FLOSEQUINAN Chemical Properties,Usage,Production

Description

Flosequinan is a new mixed arteriolar and venous vasodilator useful for the treatment of patients with congestive heart failure with or without ACE inhibitors, but especially in those patients who are intolerant to ACE inhibitors. It does not cause reflex stimulation of the renin-angiotensin or sympathetic nervous system. How flosequinan achieves its direct vasodilating effect is not clear, it is thought to interfere with protein kinase C and the production of inositol triphosphate. Flosequinan is well absorbed orally, and with the relatively long half-life of its sulfone metabolite it is suitable for once a day administration.

Originator

Boots (United Kingdom)

Uses

Antihypertensive (vasodilator).

Definition

ChEBI: Flosequinan is a member of quinolines.

Manufacturing Process

7-Fluoro-3-methylsulphinyl-4-quinolone (5.0 g) was dissolved in hot butanone (250 ml) containing anhydrous potassium carbonate (3.06 g). The resulting suspension was stirred and treated dropwise with dimethyl sulphate (2.09 ml). The mixture was stirred and boiled under reflux for 1 hour and filtered while hot. The filtrate was allowed to cool, giving a crystalline product. The product was collected and dried to give 7-fluoro-1-methyl-3-methylsulphinyl-4-quinolone, melting point 226-228°C.
The intermediate 7-fluoro-3-methylsulphinyl-4-quinolone, was prepared in the following way:
A solution of 2-amino-4-fluorobenzoic acid (62 g) in aqueous sodium carbonate (44 g sodium carbonate in 1.6 liters water) was stirred and treated dropwise with a solution of phosgene (120 g) in toluene (500 ml) during 1.5 hours. The resulting suspension was stirred at room temperature for 24 hours. The solid product was collected by filtration, washed with water and dried to give 7-fluoro-1,2-dihydro-3,1(4H)-benzoxazine-2,4-dione; melting point 217- 219°C.
A mixture of dimethyl sulphoxide (230 ml), toluene (300 ml) and 50% w/w dispersion of sodium hydride in mineral oil (20.7 g) was heated under nitrogen at 65-70°C for 1 hour, then cooled to room temperature to form dimethylsulphoxide anion, sodium salt. The resulting suspension was stirred under nitrogen and the above benzoxazine-2,4-dione (27.5 g) was added portionwise. The resulting solution was stirred at room temperature for 15 minutes and then poured into ether (3 liters). The resulting solid was collected by filtration and dissolved in water (300 ml) and the solution acidified with glacial acetic acid to a final pH of 6.0. The solution was saturated with solid potassium carbonate. The resulting precipitate was collected, dried and recrystallised from ethanol/diethyl ether to give the novel compound 2'- amino-4'-fluoro-(2-methylsulphinyl)acetophenone, melting point 115-117°C.
This compound (14 g) was dissolved in triethyl orthoformate (160 ml) at 100°C under nitrogen. The resulting solution was treated dripwise with piperidine (7 ml). The mixture was heated with stirring at 120°C under nitrogen for 30 min allowing ethanol produced to distil off, then cooled to room temperature. The solid product was collected, dried and crystalized from ethanol using charcoal to give the 7-fluoro-3-methylsulphinyl-4-quinolone; melting point 265°C.

brand name

Manoplax

Therapeutic Function

Antihypertensive, Vasodilator

FLOSEQUINAN Preparation Products And Raw materials

Raw materials

Preparation Products

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FLOSEQUINAN Suppliers

Leancare Ltd.
Tel
--
Fax
--
Email
enquiry@leancare.co.uk
Country
United Kingdom
ProdList
6446
Advantage
42
CARBONE SCIENTIFIC CO.,LTD
Tel
--
Fax
--
Email
sales@carbonesci.com
Country
United Kingdom
ProdList
6666
Advantage
30
UK GREEN SCIENTIFIC CO.,LIMITED
Tel
--
Fax
--
Email
sales@gs-chem.com
Country
United Kingdom
ProdList
6098
Advantage
47
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View Lastest Price from FLOSEQUINAN manufacturers

Shaanxi Dideu Medichem Co. Ltd
Product
Flosequinan 76568-02-0
Price
US $0.00-0.00/Kg
Min. Order
1KG
Purity
99.0%
Supply Ability
500 MT
Release date
2020-05-09

76568-02-0, FLOSEQUINANRelated Search:


  • BTS-49465
  • Flosequinon
  • Manoplax
  • 7-Fluoro-1-methyl-3-(methylsulfinyl)-4(1H)-quinolinone
  • 7-Fluoro-1-methyl-3-methylsulfinylquinolin-4(1H)-one
  • FLOSEQUINAN
  • 7-Huom-1-methyl-3-(methylsulfinyl)-4(1H)-quinolinone
  • FLOSEQUINAN USP/EP/BP
  • 4(1H)-Quinolinone, 7-fluoro-1-methyl-3-(methylsulfinyl)-
  • 76568-02-0
  • C11H10FNO2S