Teilstruktursuche

3920

O=C(CN1CCN(c2ccc(Cc3ccc(F)cc3)cc2)CC1)N1CCCOc2ccccc21
Reaction #1078
5-[2-(4-(4-(4-fluorophenyl)methylphenyl)piperazin-1-yl)acetyl]-2,3,4,5-tetrahydro-1,5-benzoxazepine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCN1CCN(c2ccc(Cc3ccc(F)cc3)cc2)CC1)N1CCCOc2ccccc21
Reaction #1081
5-[4-(4-(4-(4-fluorophenyl)methylphenyl)piperazin-1-yl)butyryl]-2,3,4,5-tetrahydro-1,5-benzoxazepine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCN1CCC(c2ccc(Cc3ccc(F)cc3)cc2)CC1)N1CCCOc2ccccc21
Reaction #1082
5-[4-(4-(4-(4-fluorophenyl)methylphenyl)piperidin-1-yl)butyryl]-2,3,4,5-tetrahydro-1,5-benzoxazepine
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)C(=O)c2ccc(NC(C)=O)cc2)c1
Reaction #2574
title compound
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)C(=O)c2ccccc2NC(C)=O)c1
Reaction #2584
title compound
Ausbeute 65.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)C(=O)c2ccc(NC(C)=O)c(C)c2)c1
Reaction #2586
title compound
Ausbeute 89.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccc(C)cc2)c1
Reaction #2590
title compound
Ausbeute 97.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccc(F)cc2)c1
Reaction #2591
title compound
Ausbeute 98.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(N(CCCN2CCC(C(=O)c3ccc(F)cc3)CC2)C(=O)c2ccc(NC(C)=O)cc2)c1
Reaction #2596
title compound
Ausbeute 96.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccc(O)c2)cc1
Reaction #2612
title compound
Ausbeute 76.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)C(=O)c2ccc(NC(C)=O)cc2)c1.O=C(O)/C=C/C(=O)O
Reaction #2620
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)C(=O)c2ccc(NC(C)=O)cc2)c1.O=C(O)C(O)C(O)C(=O)O
Reaction #2621
title compound
Ausbeute 75.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)C(=O)c2ccc(NC(C)=O)cc2)c1.O=C(O)/C=C\C(=O)O
Reaction #2622
title compound
Ausbeute 86.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCOCC2)n3Cc2ccccc2)CC1
Reaction #48121
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(-n2cnnn2)ccc1N1CCOCC1)N1CCN(c2ccc(C(F)(F)F)cc2)CC1
Reaction #60974
title compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCC(NCCSc2cccs2)CC1)C(F)(F)F
Reaction #67958
N-(2-(2-thienylthio)ethyl)-1-(trifluoroacetyl)piperidine-4-amine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)N(CCN1CCC(NCc3ccc4c(c3)OCCO4)CC1)C(=O)CC2.Cl
Reaction #68288
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-7-methoxy-3,4-dihydroquinolin-2(1H)-one hydrochloride
Ausbeute 135.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N2CCN(C(=O)C[C@@H](OC(=O)NCCc3ccccc3)c3ccccc3)CC2)cc1OC
Reaction #72490
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N(C(=S)Nc1cccc(C)c1)c1ccc(-c2ncn(-c3ccc(OC(F)(F)F)cc3)n2)cc1
Reaction #90322
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C1CCCN1c1ccc(OCCCN(CCn2ccc3ccccc3c2=O)Cc2ccncc2)cc1
Reaction #156194
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter