| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2707056d594790a62947ee030653e6f8 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C17-266
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C21-22 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C17-266 |
| filingDate |
2002-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7610b429c0063a3e7f8a02579cc80e52
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_49bdc507a353ecfc6c7d58d6bd7c78e3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_67d619bc4b0f747780044835afe00239
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ad5b4d975c74e1ccaf71c764c3db26e2 |
| publicationDate |
2004-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
KR-20040044635-A |
| titleOfInvention |
Method for preparing of allyl halide derivative |
| abstract |
The present invention relates to a method for preparing an allyl halide derivative, which is a terbinapine intermediate. In particular, an organoboron intermediate prepared by hydroboration of 1-halo-2-propine and an organoboron compound is t-butylacetyl. By reacting the inorganic inorganic salt with iodine in the presence of iodine to form a carbon-carbon coupling, it is possible to prepare a high yield of allyl halide having excellent trans-selectivity, as well as separation of the final drug terbinafine. And it relates to a method for producing an allyl halide derivative easy to purify. |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-101624328-B |
| priorityDate |
2002-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |