http://rdf.ncbi.nlm.nih.gov/pubchem/patent/IE-811968-L
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_cae71083b119f18009470b1882e54e4d |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D203-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-10 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D203-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C239-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C271-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D203-12 |
filingDate | 1981-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 1982-02-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | IE-811968-L |
titleOfInvention | Method for producing 3,6-bis(carboethoxy amino)-2,ยน5-diaziridinyl-1, 4-benzoquinone |
abstract | 3,6-bis(carboethoxyamino)-2,5-diaziridinyl-1,4-benzoquinone, sometimes known as "AZQ" is prepared by reacting a dialkylpyrocarbonate with a diamino hydroquinone to form 2,5-dichloro-3,6-bis (carboethoxyamino)-1,4-hydroquinone. The latter compound is oxidized to form the corresponding benzoquinone, which is reacted with an aziridinyl compound to produce 3,5-bis(carboethoxyamino)-2,5-diaziridinyl-1,4-benzoquinone. n[WO8200823A1] |
priorityDate | 1980-08-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 20.