http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5562072-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-62 |
| filingDate | 1978-11-01^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aa2e7bacbde34f538d3e368c97b93efb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8b011ef87de590b691fd76b5ea3aa91e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5fc415ca6eaf3690db5eb0fa71eb9856 |
| publicationDate | 1980-05-10^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-S5562072-A |
| titleOfInvention | Production of 1-substituted imidazole derivative |
| abstract | PURPOSE: An active imidazole derivative, that is, 1-substituted imidazole, is made to react with a triphenylmethanol to produce inexpensively 1-triphenylmethylimidazole that has antifungal activity using mild conditions. n CONSTITUTION: The reaction between an active imidazole derivative bearing a substitutent of formula I (R, R' are H, alkyl, cycloalkyl, or incorporate to form alkylene, or cyclic amino group containing nitrogen and oxygen atoms) in the 1-position and triphenylmethanol is effected to produce 1-triphenylmethylimidazole. The example of above 1-substituted imidazole is a compound of formula II (R 1 WR 3 are H, alkyls), which is obtained by reaction between a trialkylsilyl compound of imidazole, equimolar amount of trialkylsilyl derivative of an amine, NHR(R') and thionyl chloride. n COPYRIGHT: (C)1980,JPO&Japio |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4995898-A |
| priorityDate | 1978-11-01^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
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