http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1304588-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D265-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D223-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-227 |
| classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-22 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D223-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-227 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D265-36 |
| filingDate | 1970-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1973-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | GB-1304588-A |
| abstract | 1304588 Morpholinoalkyl benzothiazinones and related compounds E R SQUIBB & SONS Inc 26 March 1970 [1 April 1969] 14909/70 Heading C2C Compounds of the formula in which Y is -O-, -S-, -CH 2 - or -CH 2 CH 2 -, R is a C 1-7 alkyl or alkenyl, aralkyl or aralkenyl group, X and X<SP>1</SP> are each hydrogen, halogen or C 1-7 alkyl, alkoxy or haloalkyl groups, A is C 1-7 alkylene, P is 1, 2 or 3 and N=B represents an optionally substituted morpholino radical, are prepared by reacting a compound of the formula with a halide Hal-A-N = B in a dimethyl sulphoxide reaction medium, preferably in the presence of an alkali metal halide. Examples describe the preparation of benzothiazinones, benzoxazinones, dihydroquinolinones and tetrahydrobenzazepinones. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0146893-A3 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0146893-A2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4595685-A |
| priorityDate | 1969-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 24.