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fenetylline hydrochloride

CAS No.
1892-80-4
Chemical Name:
fenetylline hydrochloride
Synonyms
Biocapton;NSC 169872;Fenetylline;Fenethylline;Captagon hydrochloride;Amfetyline hydrochloride;fenetylline hydrochloride;Fenethylline hydrochloride;MVXGSLGVWBVZCA-UHFFFAOYSA-N;fenetylline hydrochloride USP/EP/BP
CBNumber:
CB0906063
Molecular Formula:
C18H24ClN5O2
Molecular Weight:
377.86846
MDL Number:
MOL File:
1892-80-4.mol
Last updated:2023-05-29 13:57:48

fenetylline hydrochloride Properties

Melting point 227-229°; mp 237-239°
solubility DMF: 0.3 mg/ml; DMSO: 0.5 mg/ml; PBS (pH 7.2): 10 mg/ml
form A crystalline solid
FDA UNII YA7K8ADZ2V
ATC code N06BA10

SAFETY

Risk and Safety Statements

Toxicity LD50 oral in rat: 100mg/kg
DEA Controlled Substances CSCN: 1503
CAS SCH: I
NARC: N

fenetylline hydrochloride Chemical Properties,Uses,Production

Originator

Captagon,Homburg,W. Germany,1961

Uses

CNS stimulant. Controlled substance.

Manufacturing Process

1 mol of 7-(β-chloroethyl)-theophylline and 2? mols of α-methyl-β-phenyl ethylamine are heated for 6 hours in an oil bath, if necessary with addition of alcohol or toluene. The reaction mixture is diluted with alcohol and acidified with alcoholic hydrochloric acid. The crystalline mass formed is filtered with suction and extracted by boiling with alcohol. A product having a melting point of 237°C to 239°C is formed. With prolonged extraction by boiling with alcohol, the melting point of the mass falls, preferably due to a change in modification, to 227°C to 229°C. However, analysis shows that both products are the pure condensation product.
Instead of the chloroethyl theophylline, it is also possible to use the corresponding bromine derivative. It was found that in this way the process is facilitated and the yield is improved

Therapeutic Function

Central stimulant

fenetylline hydrochloride Preparation Products And Raw materials

1892-80-4(fenetylline hydrochloride)Related Search:

fenetylline hydrochloride Fenethylline Fenetylline Fenethylline hydrochloride 1H-Purine-2,6-dione, 3,7-dihydro-1,3-dimethyl-7-[2-[(1-methyl-2-phenylethyl)amino]ethyl]-, monohydrochloride 7-(Phenyl-isopropyl-amino-aethyl)-theophyllin-hydrochlorid 7-[2-(1-Methyl-2-phenylethylamino)ethyl]theophylline hydrochloride 7-[2-[(.alpha.-Methylphenethyl)amino]ethyl]theophylline hydrochloride 7-[2-[(.alpha.-Methylphenethyl)amino]ethyl]theophylline monohydrochloride Amfetyline hydrochloride Captagon hydrochloride 3,7-Dihydro-1,3-diMethyl-7-[2-[(1-Methyl-2-phenylethyl)aMino]ethyl]-1H-purine-2,6-dione Hydrochloride 7-[2-[(α-Methylphenethyl)aMino]ethyl]theophylline Hydrochloride Biocapton NSC 169872 MVXGSLGVWBVZCA-UHFFFAOYSA-N fenetylline hydrochloride USP/EP/BP 1892-80-4 C18H24ClN5O2 Amines Aromatics Bases & Related Reagents Intermediates & Fine Chemicals Nucleotides Pharmaceuticals