http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1181069-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_4c4cb9b5558ad97d3acc0db1113f7727 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D241-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D295-096 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-096 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D241-08 |
filingDate | 1981-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 1985-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a33403de2826f0332961c92539fc5847 |
publicationDate | 1985-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CA-1181069-A |
titleOfInvention | Process for preparing 1-(trialkoxybenzyl) piperazines |
abstract | SPECIFIC The invention relates to the preparation of (trialcoxy benzyl) -1 piperazines and in particular of (2,3,4,4-trimethoxy benzyl) -1 piperazine. the process consists in preparing, in a first phase, the piperazinone-2 corresponding to said piperazine, then to reduce, in a second phase, said piperazinone. More specifically, in the first phase, a mole is reacted in a first solvent of a trialkoxy benzyl chloride on two moles of piperazinone-2 to obtain a trialcoxy benzyl-4 piperazinone-2 and, in the second phase, we reduce this last compound, in a second solvent, using a hydride. preferably the first solvent is toluene, the second solvent tetrahydrofuran and said hydride AlLiH4 or B2H6. (no drawing) |
priorityDate | 1980-11-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 34.