SU163181A1 - - Google Patents

Info

Publication number

SU163181A1

SU163181A1 SU777616A SU777616A SU163181A1 SU 163181 A1 SU163181 A1 SU 163181A1 SU 777616 A SU777616 A SU 777616A SU 777616 A SU777616 A SU 777616A SU 163181 A1 SU163181 A1 SU 163181A1

Authority

SU

USSR - Soviet Union

Prior art keywords

mixture

schiff bases

derivatives

mol

toluenesulfonic acid

Prior art date

Links

• Espacenet
• Global Dossier
• Discuss

• 238000000034 method Methods 0.000 description 5
• 150000003248 quinolines Chemical class 0.000 description 5
• UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
• 239000002262 Schiff base Substances 0.000 description 3
• 150000004753 Schiff bases Chemical class 0.000 description 3
• 239000000203 mixture Substances 0.000 description 3
• VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
• 229940027991 antiseptic and disinfectant quinoline derivative Drugs 0.000 description 2
• 238000006243 chemical reaction Methods 0.000 description 2
• 125000005670 ethenylalkyl group Chemical group 0.000 description 2
• JBIJLHTVPXGSAM-UHFFFAOYSA-N 2-naphthylamine Chemical compound C1=CC=CC2=CC(N)=CC=C21 JBIJLHTVPXGSAM-UHFFFAOYSA-N 0.000 description 1
• ZXTHWIZHGLNEPG-UHFFFAOYSA-N 2-phenyl-4,5-dihydro-1,3-oxazole Chemical compound O1CCN=C1C1=CC=CC=C1 ZXTHWIZHGLNEPG-UHFFFAOYSA-N 0.000 description 1
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
• 150000001299 aldehydes Chemical class 0.000 description 1
• 125000003545 alkoxy group Chemical group 0.000 description 1
• 125000000217 alkyl group Chemical group 0.000 description 1
• 229940111121 antirheumatic drug quinolines Drugs 0.000 description 1
• 150000004982 aromatic amines Chemical class 0.000 description 1
• 125000003118 aryl group Chemical group 0.000 description 1
• 239000002585 base Substances 0.000 description 1
• -1 benzylidene- Chemical class 0.000 description 1
• 150000001875 compounds Chemical class 0.000 description 1
• 230000005494 condensation Effects 0.000 description 1
• 238000009833 condensation Methods 0.000 description 1
• 238000010438 heat treatment Methods 0.000 description 1
• RDOWQLZANAYVLL-UHFFFAOYSA-N phenanthridine Chemical compound C1=CC=C2C3=CC=CC=C3C=NC2=C1 RDOWQLZANAYVLL-UHFFFAOYSA-N 0.000 description 1
• 125000001424 substituent group Chemical group 0.000 description 1