Buflomedil hydrochloride
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Buflomedil hydrochloride
structure -
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CAS No:
35543-24-9
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Formula:
C17H25NO4.ClH
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Chemical Name:
Buflomedil hydrochloride
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Synonyms:
1-Butanone,4-(1-pyrrolidinyl)-1-(2,4,6-trimethoxyphenyl)-,hydrochloride (1:1);1-Butanone,4-(1-pyrrolidinyl)-1-(2,4,6-trimethoxyphenyl)-,hydrochloride;LL 1656;Buflomedil hydrochloride;Irrodan R;Fonzylane;Buflocit;Lofton;Buflan;Provas;Loftyl;Bufedil;Irrodan;Buflonat;1-[3-(2,4,6-Trimethoxybenzoyl)Propyl]PyrrolidiniumChloride
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Categories:
Active Pharmaceutical Ingredients > Circulatory System Drugs
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CAS No:
Description
Buflomedil HCl is a vasodilator used to treat claudication or the symptoms of peripheral arterial disease.Target: OthersBuflomedil is a vasoactive drug used to treat claudication or the symptoms of peripheral arterial disease. In the EU, buflomedil, a vasoactive agent, was indicated for treatment of PAOD symptoms, specifically in patients with stage II PAOD who experience severe pain when walking even relatively short distances. Buflomedil is not currently approved by the US Food and Dru
Characteristics
48
3.51100
White or off-white crystalline powder
192-193 °C
454.5°C at 760 mmHg
228.7ºC
Oral-rat LD50: 410 mg/kg; Oral-Mouse LD50: 275 mg/kg
Thermal decomposition releases toxic nitrogen oxides and hydrogen chloride fumes
Safety Information
NONH for all modes of transport
3
EL9885000
The warehouse is ventilated, low temperature and dry; stored separately from food raw materials
P264, P270, P301+P312, P330, P501
H302
Buflomedil hydrochloride Use and Manufacturing
In a separate dry reaction flask, 33.6 g of 1, 3, 5-trimethoxybenzene and 27.2 g of anhydrous zinc chloride were added.Dichloromethane 300mL, stirring and cooling to 0-5 degrees after dropping 36.5g 1-pyrrolidinoyl chloride, drops, The reaction was heated to reflux for 2 hours. After the reaction was complete, 15 mL of concentrated hydrochloric acid and 150 mL of pure water were added and washed.The resulting organic phase is washed with saturated sodium bicarbonate solution to a pH of 7-8, and the organic phase is dried over magnesium sulfate and then reduced to dryness.Add 100 mL of anhydrous ethanol to the concentrate.20percent hydrochloric acid ethanol100mLAfter stirring the reaction at 60-70°C for 1 hour, the ethanol is then reduced to dryness.After adding 400 mL of acetone to the residue and cooling and crystallizing, the white crystal was filtered to obtain 60.2 g of buflomedil hydrochloride.
Buflomedil is used as an vasodilator (peripheral).
Drug Function and Efficacy
It is an α-adrenergic receptor inhibitor and has a weak nonspecific calcium ion antagonist effect. It improves the microcirculation blood flow in the brain and limbs by inhibiting the spasm of the precapillary sphincter. It also has the function of inhibiting platelet aggregation and improving red blood cell deformability.
Registered Holders
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ISOCHEM
Active
France
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ISOCHEM Vert Le
Active
European Union
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AMDIPHARM LIMITED
Inactive
European Union
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