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filingDate 2000-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_406c1a0b995cebeac5abc8942fc937b4
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publicationDate 2001-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber PE-20010052-A1
titleOfInvention AZEPININDOL TETRACYCLIC COMPOUNDS AS AGONISTS OR ANTAGONISTS OF THE 5-HT RECEPTOR
abstract REFERS TO DERIVATIVES OF 1,2,3,4,5,6-HEXAHIDROAZEPIN- [4,5-b] INDOLE THAT HAVE A RING TO JOIN POSITION 6 AND 7 OF FORMULA I WHERE R1 IS OH, NITRO, HALOGEN, CN, TRIFLUOROMETHYL, S (O) mNRaRb, NRcRd, S (O) mRe, AMONG OTHERS; R2 IS H, C1-C7 ALKYL, C1-C7 ALKANOYL, C1-C7 ALCOXYCARBONYL, AMONG OTHERS; X AND Y TOGETHER ARE A CHAIN WITH C ATOMS OPTIONALLY CONTAINING A GROUP -O-, -S-, -SO-, -SO2-, NRf OPTIONALLY SUBSTITUTED WITH OXO, OH, C1-C7 ALCOXYL; m IS 0-2; n IS 0-3; EACH Ra AND Rb ARE H, C1-C7 ALKYL, ARYL, C1-C7 ARYLALKYL, HETEROARYL, C1-C7 HETEROARYL ALKYL; Ra AND Rb TOGETHER WITH N FORM PYRROLIDINE, PIPERIDINE, MORFOLINO, THIOMORFOLINO; EACH Rc AND Rd ARE H, C1-C7 ALKYL, C1-C7 ALKANOYL, C1-C7 ALCOXYCARBONYL, ARYL, OR TOGETHER WITH N FORMING PYRROLIDINE, PIPERIDINE, MORPHOLINE, THYOMORPHOLIN, AMONG OTHERS; Re IS H, C1-C7 ALKYL, ARYL, AMONG OTHERS; Rf IS H, C1-C7 ALKYL, ARYL, C1-C7 ARYLALKYL, AMONG OTHERS; WITH THE CONDITION THAT AND IS NOT OXY, TIO, SULFINIL, NRf, AMONG OTHERS. PREFERRED COMPOUNDS ARE 5,6,9,10,11,12-HEXAHYDRO-4H, 8H-AZEPIN [4`, 5 ': 4.5] PYRROL [3,2,1-ij] QUINOLINE, 2-METHYL-5 , 6,9,10,11,12-HEXAHYDRO-4H, 8H-AZEPIN [4 ', 5': 4.5] PYRROL [3,2,1-ij] -QUINOLINE, AMONG OTHERS. COMPOUNDS I ARE BINDERS OF SEROTONIN 5-HT AND MAY BE USEFUL FOR THE TREATMENT OF DISEASES OF THE CENTRAL NERVOUS SYSTEM, DREAM, DEPRESSION
priorityDate 1999-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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