http://rdf.ncbi.nlm.nih.gov/pubchem/patent/IL-204000-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_981a37900e6991fb373304ed2ba5a703 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-61 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-60 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B61-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D- |
| filingDate | 2010-02-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2013-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | IL-204000-A |
| titleOfInvention | METHOD OF CREATING HISTORY 2, 2 - RELIABLE ETHYL DIPLURO THROUGH EIMIN FUNDING |
| abstract | Preparing 2,2-difluoroethylamine-derivatives comprises hydrogenating 2,2-difluoroethylimine-derivative (IV) to the corresponding 2,2-difluoroethylamine-derivative (III). Preparing 2,2-difluoroethylamine-derivatives comprises hydrogenating 2,2-difluoroethylimine-derivative of formula (A-CH 2=N-CH 2-C(F) 2) (IV) to the corresponding 2,2-difluoroethylamine-derivative of formula (A-CH 2-NH-CH 2-C(F) 2) (III). A : pyrid-2-yl, pyrid-4-yl or pyrid-3-yl (all optionally substituted by F, Cl, Br, CH 3, CF 3or CF 3O (at 6th position)) or pyridazin-3-yl (optionally substituted by Cl or CH 3(at 6th position)), and pyrazin-3-yl, 2-chloropyrazin-5-yl or 1,3-thiazol-5-yl (all optionally substituted by Cl or CH 3(at 2nd position)), or pyrimidinyl, pyrazolyl, thiophenyl, oxazolyl, isoxazolyl, 1,2,4-oxadiazolyl, isothiazolyl, 1,2,4-triazolyl or 1,2,5-thiadiazolyl (all optionally substituted by F, Cl, Br, CN, NO 2, 1-4C-alkyl (optionally substituted by F and/or Cl), 1-3C-alkylthio (optionally substituted by F and/or Cl), 1-3C-alkylsulfonyl (optionally substituted by F and/or Cl)) or substituted pyridine moiety of formula (A1); X : halo, alkyl or haloalkyl; and Y 1>halo, alkyl, haloalkyl, haloalkoxy, azido or cyano-group. Independent claims are included for: (1) preparing 2,2-difluoroethylimine-derivative of formula (IV) comprising reacting a carbonyl compound of formula (A-C(=O)-H) (VI) with 2,2-difluoroethylamine; and (2) the 2,2-difluoroethylimine-derivative (IV). [Image] |
| priorityDate | 2007-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 143.