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863176

COCCN(C(=O)n1cc[n+](C)c1)c1ccc(F)cc1.[I-]
Reaction #532556
1-((4-Fluorophenyl)(2-methoxyethyl)carbamoyl)-3-methyl-1H-imidazol-3-ium iodide
DOI: 10.6084/m9.figshare.5104873.v1
COCCN(C(=O)N1CCc2ccccc2[C@H]1c1ccc(C(F)(F)F)cc1)c1ccc(F)cc1
Reaction #532557
(R)—N-(4-fluorophenyl)-N-(2-methoxyethyl)-1-(4-(trifluoromethyl)phenyl)-3,4-dihydroisoquinoline-2(1H)-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
C[n+]1ccn(C(=O)N(CCN2C(=O)c3ccccc3C2=O)c2ccc(F)cc2)c1.[I-]
Reaction #532560
product
Ausbeute 99.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCN(C(=O)N1CCc2ccccc2[C@H]1c1ccc(C(F)(F)F)cc1)c1ccc(F)cc1
Reaction #532561
(R)—N-(2-(1,3-dioxoisoindolin-2-yl)ethyl)-N-(4-fluorophenyl)-1-(4-(trifluoromethyl)-phenyl)-3,4-dihydroisoquinoline-2(1H)-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
C[n+]1ccn(C(=O)N2CCCc3ccccc32)c1.[I-]
Reaction #638972
1-(3,4-Dihydroquinolin-1(2H)-ylcarbonyl)-3-methyl-1H-imidazol-3-ium Iodide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(C(=O)N2CCCc3ccccc32)CC1
Reaction #638973
Ethyl 1-(3,4-dihydroquinolin-1(2H)-ylcarbonyl)piperidine-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Oc1ccc(N2C(=O)CC(C)(C)CC2=O)cc1)c1ccccc1
Reaction #1266910
title product
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Oc1ccc(N2C(=O)[C@H]3CCCC[C@H]3C2=O)cc1)c1ccccc1
Reaction #1266911
title compound
Ausbeute 77.4%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Oc1ccc(NC(=O)C2CCCCC2)cc1)c1ccccc1
Reaction #1266912
title compound
Ausbeute 80.3%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Oc1ccc(NC(=O)CC2CCCCC2)cc1)c1ccccc1
Reaction #1266913
title compound
Ausbeute 77.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Oc1ccc(NC(=O)[C@H]2CC[C@H](C(C)(C)C)CC2)cc1)c1ccccc1
Reaction #1266914
title compound
Ausbeute 86.4%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Oc1ccc(NC(=O)CC(C)(C)C)cc1)c1ccccc1
Reaction #1266915
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cc2ccccc2)c(=O)oc2cc(OC(=O)N(C)c3ccccc3)ccc12
Reaction #1266916
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cc2ccc(Cl)c(Cl)c2)c(=O)oc2cc(OC(=O)N(C)c3ccccc3)ccc12
Reaction #1266917
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cc2c(F)cccc2Cl)c(=O)oc2cc(OC(=O)N(C)c3ccccc3)ccc12
Reaction #1266918
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cc2c(Cl)cccc2Cl)c(=O)oc2cc(OC(=O)N(C)c3ccccc3)ccc12
Reaction #1266919
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cc2c(Cl)cccc2Cl)c(=O)oc2cc(OC(=O)N(C)c3ccccc3)c(Cl)cc12
Reaction #1266920
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2c(C)c3ccc(OC(=O)N(C)c4ccccc4)cc3oc2=O)cc1
Reaction #1266921
title compound
Ausbeute 43.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(=O)oc2cc(OC(=O)N(C)c3ccccc3)ccc12
Reaction #1266922
title compound
Ausbeute 62.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(OC)c(-c2c(C)c3ccc(OC(=O)N(C)c4ccccc4)cc3oc2=O)c1
Reaction #1266923
title compound
Ausbeute 13.5%DOI: 10.6084/m9.figshare.5104873.v1
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