http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2007147925-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P37-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P19-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P27-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-47 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D491-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P3-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D491-048 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D491-052 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P17-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-02 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-04 |
| filingDate | 2006-05-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2009-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | RU-2007147925-A |
| titleOfInvention | Substituted Tetrahydroquinolines |
| abstract | 1. The compounds of formula I! ! wherein ! W represents SI or N,! R1, R2, R3, independently of one another, are H, A, aryl, heteroaryl, Hal, - (CY2) n-SA, - (CY2) n-SCF3, - (CY2) n-SCN, - (CY2 ) n-CF3, - (CY2) n-OCF3, R, NR-NR2, X (CY2) nXR, X (CY2) nY, (СY2) n-cycloalkyl,! (CY2) nCH = CH2, cycloalkyl, -SCH3, -SCN, -CF3, -OCF3, -OA, - (CY2) n-OH, - (CY2) n-CO2R, - (CY2) n-CN, - ( CY2) n-Hal, - (CY2) nY, - (CY2) nRa,! - (CY2) n-NR2, (CY2) n-OA, (CY2) n-OCOA, -SCF3, (CY2) n-CONR2, - (CY2) n-NHCOA, - (CY2) n-NHSO2A, SF3, 5; (CH3) 3, CO- (CY2) n-CH3, - (CY2) n-pyrrolidone. (CH2) nNRCOOR, NRCOOR, NCO,! (CH2) nCOOR, NCOOR, (CH2) nOH, NR (CH2) nNR2, C (OH) R2,! NR (CH2) nOR, NCOR, (CH2) n-aryl, (CH2) n-heteroaryl, (CH2) nR1,! (CH2) nX (CH2) n-aryl, (CH2) nX (CH2) n-heteroaryl, (CH2) nCONR2,! XCONR (CH2) nNR2, N [(CH2) nXCOOR] CO (CH2) n-aryl,! N [(CH2) nXR] CO (CH2) n-apyl,! N [(CH2) nXR] CO (CH2) nX-apyl,! N [(CH2) nXR] SO2 (CH2) n-aryl, N [(CH2) nNRCOOR] CO (CH2) n-aryl,! N [(CH2) nNR2] CO (CH2) n-aryl,! N [(CH2) nNR2] CO (CH2) nNR-aryl,! N [(CH2) nNR2] SO2 (CH2) n-aryl,! N [(CH2) nXR] CO (CH2) n-heteroaryl, N [(CH2) nXR] CO (CH2) nX-heteroaryl, CO-aryl, SO2-aryl, N [(CH2) nXR] SO2 (CH2) n heteroaryl! N [(CH2) nNRCOOR] -CO (CH2) n-heteroaryl,! N [(CH2) nNR2] CO (CH2) n-heteroaryl,! N [(CH2) nNR2] CO (CH2) nNR-heteroaryl, R1 and R3 together also represent -NC (CF3) = N-, -N-CR = N-, -NN = N-, and where non-adjacent CY2 groups X can also be replaced! Y represents H, A, Hal, OR, E-R1,! E represents -NR1SO2-, -SO2NR1-, -CONR1-, -NR1CO-, -СОО-, ООС-, СО, -SO2-, -Х-, NR1CONR1-, -OCONR1-, -NR1COO-, -CSNR1- , -NR1CS-, -NR1CSNR1-, -SCONR1-, -NR1COS-, -OCSNR1-, NR1CSO-, SCSNR1-, -NR1CSS or a simple connection! A is alkyl or cycloalkyl in which one or more hydrogen atoms can be replaced by Hal,! Hal represents F, Cl, Br or I,! R represents H or A, in the case of geminal radicals R together also - (CH2) 5-, - (CH2) 4-, or - (CH2) n-X- (CH2) n, or - (CH2) nZ- ( CH2) n,! R4, R4 ',! R5, R5 ', independently of one another, are H or unsubstituted or single or poly-OR-, -NO2-, -Hal-, -CF3-, -OCF3-, -CN-, -NR2- or -SR -, -aryl- or -heteroaryl-substituted N-pyrrolidone, Q, - (CY2) nE -CR2R1, - (CY2) nE-CR2XR1, - (CY2) nE- (CY2) n-XR1 or - (CY2) n - (CY2) n-XRa-X- (CH2) 2OR, -X-CO (CH2) nCH3, -X- (CH2) 2NR2, R1, S-aryl, O |
| priorityDate | 2005-06-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 72.