http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1301886-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/D06M13-35 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-28 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/D06M13-35 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-28 |
| filingDate | 1970-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1973-01-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | GB-1301886-A |
| abstract | 1301886 2-Carbamylimidazolines BADISCHE ANILIN- & SODA-FABRIK AG 24 April 1970 [26 April 1969] 19805/70 Heading C2C [Also in Division D1] Novel imidazolines of the formula in which R 1 , R 2 and R3 are hydrogen or aliphatie or cycloaliphatic groups and R 3 may also be an aromatic or araliphatic group or R 2 and R 3 may together complete a heterocyclic ring, are prepared by reacting a haloacetamide of the formula with a diamine of the formula and elemental sulphur. The reaction is preferably effected at 50-180‹ C. using an excess of the diamine reactant or in the presence of another base capable of binding, the acid HX formed. Examples relate to the preparation of 2-(N- butylcarbamyl) -, 2 - (N - 3 - chloro - 4 - methylphenylcarbamyl) -, 2 - (N - dodecylcarbamyl)., 2-(N - 2,4 - dichlorophenylcarbamyl)-, 2-(N- benzylcarbamyl)-, 2 - (N - isopropylcarbamyl)- and 2 - (N - cyclohexylcarbamyl)- imidazolines. The compounds are used in textile finishing (see Division D1). |
| priorityDate | 1969-04-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 18.