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655-35-6

655-35-6 Structure

655-35-6 Structure
IdentificationBack Directory
[Name]

CARBOCROMENE HYDROCHLORIDE
[CAS]

655-35-6
[Synonyms]

Carboc
antiangor
Aids126445
Aids-126445
Karbokromen
intercordin
carbocromene
chromonar HCl
intensain hydrochloride
CARBOCROMENE HYDROCHLORIDE
CarbochroMen Hydrochloride
carbochromene hydrochloride
3-(beta-diethylaminoethyl)-4-methyl-7-(carbethoxymethoxy)-coumarin hydrochlor
3-(2-DiethylaMinoethyl)-4-Methyl-7-carbethoxyMethoxy -2-oxo-1,2-chroMene Hydrochloride
3[2-(N,N-Diethylamino)ethyl]-4-methyl-2-oxo-2H-1-benzopyran-7-yloxyacetic acid ethanol ether
ethyl 2-({3-[2-(diethylamino)ethyl]-4-methyl-2-oxo-2H-c hromen-7-yl}oxy)acetate hydrochloride
ethyl [[3-[2-(diethylamino)ethyl]-4-methyl-2-oxo-2H-1-benzopyran-7-yl]oxy]acetate hydrochloride
2-[[3-[2-(DiethylaMino)ethyl]-4-Methyl-2-oxo-2H-1-benzopyran-7-yl]oxy]acetic Acid Ethyl Ester Hydrochloride
Acetic acid, {[[3-[2-(diethylamino)ethyl]-4-methyl-2-oxo-2H-1-benzopyran-7-yl]ox} Y\]-, ethyl ester, hydrochloride
[EINECS(EC#)]

211-511-5
[Molecular Formula]

C20H28ClNO5
[MOL File]

655-35-6.mol
[Molecular Weight]

397.893
Chemical PropertiesBack Directory
[Melting point ]

159-160°
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethyl bromoacetate
Hazard InformationBack Directory
[Originator]

Intensain,Hoechst,Switz,1963
[Uses]

Vasodilator (coronary).
[Definition]

ChEBI: Carbocromen hydrochloride is a member of coumarins.
[Manufacturing Process]

18.7 g of 3β-diethylaminoethyl-4-methyl-7-hydroxy-coumarin chlorhydrate are dissolved in 200 cc methyl ethyl ketone and 18 g anhydrous potassium carbonate are added. The mixture is stirred for 1 hour at 70°C and then 12 g bromoacetic acid ethyl ester are allowed to drop in. The reaction mixture is stirred under reflux for 9 hours and then it is filtered off with suction in the heat. The filtrate is concentrated in the vacuum to dryness and the resultant
residue is dissolved in ether. The etheric solution is washed with diluted caustic soda solution for several times and, subsequently, dried with Glauber's salt. By introduction of hydrochloric acid gas into the etheric solution the reaction product is precipitated in the form of chlorhydrate. Yield: 15 g of 3β- diethylaminoethyl-4-methylcoumarin-7-ethyl oxyacetate chlorhydrate having a melting point of 154° to 156°C (= 63% of the theory).
The starting material is produced by reacting resorcinol with 2-(2- diethylaminoethyl)acetic acid ethyl ester.
[Therapeutic Function]

Coronary vasodilator
Safety DataBack Directory
[Toxicity]

LD50 in mice (g/kg): 6.3 orally; 0.528 i.p.; 0.0355 i.v. (Nitz, Potzch)
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