H. A^-methyI*2-nitroacetamide,
ASSAY
Dissolve 0.280 g in 35 ml of wałer R. Titrate with 0.1 M sodium hydroxide, determining the end-point potentiometrically (2.2.20).
1 ml of 0.1 M sodium hydroxide is equivalent to 35.09 mg of CjjH^CIN^OjS.
STORAGE
In airtight Container, protected from UghL IMPURITIES
Specified impuriłies: A, B, C, D, E, F, G, H, I, J.
Other deteciable impuriłies: K.
CH3
h3c-n
A. A^Ar-bis[2-[[[5-((dimethylamino)methyl]furan-2-yl]methyl]sulphanyl]ethyl]-2-nitroethene-l,l-diamine,
I. 2,2/-methylenebis[A42-{[[5-((dirnethylamino)methyl]furan-2-yl]methyl]sulphanyl]ethyl]-Ar-methyb2-nitroethene-l,l-diamine],
J. l,r-A4methylenebis(sulphanediyIethylene)]bis(Ar-methyl-2-nitroethene-l,l-diamine),
H
B. R = S-CH2-CH2-NH2: 2-[[[5-{(dimethylamino)methyl]furan-2-yl]methyI]sulphanyl]ethanamine,
D. R = SCH2-CH2-NH-COCH2-N02: Aq2-[[I5-[(dimethyl-amino)methyl]furan-2-yI]methyl]sulphanyl]ethyI]-2-ni-troacetamide,
F. R = OH: [5-[(dimethylamino)methyl]furan-2-yl]methanol,
K. A^-methyl-l-methylthio-2-nitroethenamine.
Działanie i zastosowanie.
Antagonista receptorów H2 stosowany w chorobie wrzodowej żołądka i dwunastnicy oraz w zespołach przebiegających z nadmiernym wydzielaniem soku żołądkowego.
C. A/’-[2-[[[5-{(dimethylamino)methyl]furan-2-
yllmethyllsulphinyljethylJ-A^-methyl^-nitroethene-l,!-
diamine,
E. A42-{[[54(dimethyloxidoamino)methyl]furan-2-
yl]methyl]sulphanyl]ethyl}-A^-methyl-2-nitroethene-l,l-
diamine,
H
G. 3-(methylamino)-5,6-dihydro-2//-l,4-thiazin-2-on6-oxirne,