ChemicalBook--->CAS DataBase List--->91-79-2

91-79-2

91-79-2 Structure

91-79-2 Structure
IdentificationBack Directory
[Name]

thenyldiamine
[CAS]

91-79-2
[Synonyms]

Tenfidil
Thefanil
WIN-2848
Thenfadil
thenyldiamine
thenyldiamine USP/EP/BP
Thenyldiamine Hydrochloride (Thenfadil)
N,N-dimethyl-N-2-pyridyl-N-3-thenylethylenediamine
2-dimethylaminoethyl-(2-pyridyl)-(3-thienylmethyl)amine
N,N-Dimethyl-N'-(2-pyridinyl)-N'-(3-thienylmethyl)-1,2-ethanediamine
1,2-Ethanediamine, N1,N1-dimethyl-N2-2-pyridinyl-N2-(3-thienylmethyl)-
N',N'-dimethyl-N-pyridin-2-yl-N-(thiophen-3-ylmethyl)ethane-1,2-diamine
[EINECS(EC#)]

202-098-2
[Molecular Formula]

C14H19N3S
[MDL Number]

MFCD00242574
[MOL File]

91-79-2.mol
[Molecular Weight]

261.39
Chemical PropertiesBack Directory
[Boiling point ]

bp1.0 169-172°
[density ]

1.1388 (rough estimate)
[refractive index ]

nD20 1.5915
[pka]

pKa 3.94(H2O t=25 c=0.002 to 0.01) (Uncertain);8.93 (Uncertain)
[Water Solubility ]

4.444g/L(37.5 ºC)
Safety DataBack Directory
[Hazardous Substances Data]

91-79-2(Hazardous Substances Data)
Hazard InformationBack Directory
[Chemical Properties]

Liquid.
[Originator]

Thenyldiamine,ZYF Pharm Chemical
[Uses]

Medicine (as base for various salts, especially the hydrochloride).
[Definition]

ChEBI: Thenyldiamine is a dialkylarylamine and a tertiary amino compound.
[Manufacturing Process]

To a suspension of 3.12 g of sodium amide in 50 ml dry toluene was added dropwise 12 g of 2-(dimethylamino)ethylaminopyridine. The mixture was refluxed for 2 hours, cooled to 50°C, and 21 g 3-thenyl bromide was added dropwise. When reaction subsided, the brownish-orange mixture was refluxed for 0.5 hour, cooled, and poured into 150 ml of water. The toluene layer was separated, extracted with 5% hydrochloric acid. This extract was saturated with potassium carbonate. The free base was extracted with ether, dried and fractionated. Yield of N,N-dimethyl-N'-2-pyridinyl-N'-(3-thienylmethyl)-1,2- ethanediamine 31%, boiling point 169-172°C/1 mm.
106 g of the free base was dissolved in 500 ml of isopropyl alcohol and 34 ml concentrated hydrochloric acid was added. After shaking, the reaction mixture was allowed to added. After through cooling in an ice-methanol mixture, the salt was collected and washed on the filter with low boiling petroleum ether, Melting point of N,N-dimethyl-N'-2-pyridinyl-N'-(3-thienylmethyl)-1,2- ethanediamine hydrochloride 169.5-170°C.
[Therapeutic Function]

Antihistaminic
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