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hexobendine

Product Name
hexobendine
CAS No.
54-03-5
Chemical Name
hexobendine
Synonyms
Hexabendin;Hexobendin;Hexabendine;hexobendine;KRQAMFQCSAJCRH-UHFFFAOYSA-N;N,N'-Dimethyl-N,N'-bis[3-(3,4,5-trimethoxybenzoyloxy)propyl]ethylenediamine;Benzoic acid, 3,4,5-trimethoxy-, 1,1'-[1,2-ethanediylbis[(methylimino)-3,1-propanediyl]] ester;3-[methyl-[2-[methyl-[3-(3,4,5-trimethoxybenzoyl)oxypropyl]amino]ethyl]amino]propyl 3,4,5-trimethoxybenzoate;3-[methyl-[2-[methyl-[3-(3,4,5-trimethoxyphenyl)carbonyloxypropyl]amino]ethyl]amino]propyl 3,4,5-trimethoxybenzoate;3,4,5-trimethoxybenzoic acid 3-[methyl-[2-[methyl-[3-(3,4,5-trimethoxybenzoyl)oxypropyl]amino]ethyl]amino]propyl ester
CBNumber
CB0886402
Molecular Formula
C30H44N2O10
Formula Weight
592.68
MOL File
54-03-5.mol
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hexobendine Property

Melting point:
75-77°
pka
pKa 4.52 ± 0.01;8.47 ± 0.01(H2O,t = 25.0±0.1,I=0.1,N2)(Approximate)
CAS DataBase Reference
54-03-5
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Hazard and Precautionary Statements (GHS)

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hexobendine Chemical Properties,Usage,Production

Originator

Reoxyl,Hormonchemie,W. Germany,1966

Uses

Vasodilator .

Definition

ChEBI: Hexobendine is a trihydroxybenzoic acid.

Manufacturing Process

Methylacrylate and N,N'-dimethylethylenediamine are first reacted and that product reduced with lithium aluminum hydride to give a compound A.
To a solution of 13 parts of compound A and 12 parts by volume of absolute pyridine in 80 parts by volume of absolute dioxane there are added dropwise and under constant stirring 35 parts of 3,4,5-trimethoxybenzoyl chloride dissolved in 70 parts by volume of absolute dioxane in the course of 30 minutes. The mixture is stirred for a further 3 hours at a temperature of 100°C and the excess solvent is then evaporated in vacuo. The residue of the evaporation is treated with ethyl acetate and saturated sodium carbonate solution, whereafter the organic phase is separated, treated with water, dried with sodium sulfate and the solvent is removed in vacuo. The residue thus obtained is taken up in ether and separated from 4 parts of insoluble trimethoxybenzoic acid anhydride by filtration. After evaporation of the ether there are obtained 32.5 parts of N,N'-dimethyl-N,N'-bis-[3-(3,4,5- trimethoxybenzoxy)propyl]-ethylene diamine, corresponding to a yield of 86% of the theoretical. MP: 75°C to 77°C.
The di-tertiary base thus obtained is dissolved in ether and the solution is saturated with hydrogen chloride gas. After isolation and reprecipitation from methanol-ether there is obtained the dihydrochloride melting at 170°C to 174°C.

Therapeutic Function

Vasodilator

hexobendine Preparation Products And Raw materials

Raw materials

Preparation Products

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hexobendine Suppliers

2A PharmaChem USA
Tel
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Fax
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Email
sales@2apharmachem.com
Country
United States
ProdList
6137
Advantage
39
3B Scientific Corporation
Tel
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Fax
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Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
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54-03-5, hexobendine Related Search:


  • hexobendine
  • Hexabendin
  • Hexabendine
  • Hexobendin
  • N,N'-Dimethyl-N,N'-bis[3-(3,4,5-trimethoxybenzoyloxy)propyl]ethylenediamine
  • 3,4,5-trimethoxybenzoic acid 3-[methyl-[2-[methyl-[3-(3,4,5-trimethoxybenzoyl)oxypropyl]amino]ethyl]amino]propyl ester
  • 3-[methyl-[2-[methyl-[3-(3,4,5-trimethoxybenzoyl)oxypropyl]amino]ethyl]amino]propyl 3,4,5-trimethoxybenzoate
  • 3-[methyl-[2-[methyl-[3-(3,4,5-trimethoxyphenyl)carbonyloxypropyl]amino]ethyl]amino]propyl 3,4,5-trimethoxybenzoate
  • KRQAMFQCSAJCRH-UHFFFAOYSA-N
  • Benzoic acid, 3,4,5-trimethoxy-, 1,1'-[1,2-ethanediylbis[(methylimino)-3,1-propanediyl]] ester
  • 54-03-5
  • C30H44N2O10