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1377949

COC(=O)c1cc(F)c(F)c2c1NC(C)CC2
Reaction #10437
title compound
Ausbeute 68.9%DOI: 10.6084/m9.figshare.5104873.v1
Cn1nnnc1NC(=O)c1cccc2cccnc12
Reaction #54173
8-(1-methyl-1H-tetrazole-5-yl-carbamoyl)quinoline
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2cccnc2c1C(=O)Nc1nnn[nH]1
Reaction #54174
7-methyl-8-(1H-tetrazole-5-ylcarbamoyl)quinoline
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c2cccc(C(=O)Nc3nnn[nH]3)c2n1
Reaction #54175
2,4-dimethyl-8-(1H-tetrazole-5-ylcarbamoyl)quinoline
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2ccc(NC(=O)c3ccc(-c4c(Cl)c(OC)cc(OC)c4Cl)c4cccnc34)cc2)CC1
Reaction #71469
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)cc(-c2ccc(C(=O)O)c3ncccc23)c1
Reaction #71470
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(Br)c2cccnc12
Reaction #71471
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3cnc[nH]3)c3ncccc23)c1Cl
Reaction #71475
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3ccc(CN4CCN(C)CC4)cn3)c3ncccc23)c1Cl
Reaction #71476
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2ccc(NC(=O)c3ccc(-c4c(Cl)c(OC)cc(OC)c4Cl)c4cccnc34)nc2)CC1
Reaction #71477
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CCN(Cc3ccc(NC(=O)c4ccc(-c5c(Cl)c(OC)cc(OC)c5Cl)c5cccnc45)nc3)CC2)cc1
Reaction #71478
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3ccc(CN4CCN(C)CC4)nc3)c3ncccc23)c1Cl
Reaction #71480
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2ccc(NC(=O)c3ccc(-c4c(Cl)c(OC)cc(OC)c4Cl)c4cccnc34)cn2)CC1
Reaction #71481
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CCN(Cc3ccc(NC(=O)c4ccc(-c5c(Cl)c(OC)cc(OC)c5Cl)c5cccnc45)cn3)CC2)cc1
Reaction #71482
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(F)c(-c2ccc(C(=O)Nc3ccc(CN4CCN(C)CC4)cn3)c3ncccc23)c1F
Reaction #71486
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(-c2cc(OC)cc(OC)c2)c2cccnc12
Reaction #71487
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)O)c3ncccc23)c1F
Reaction #71489
title compound
Ausbeute 96.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(-c2c(F)c(OC)cc(OC)c2Cl)c2cccnc12
Reaction #71490
title compound
Ausbeute 66.2%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #89058
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(-c2ccccc2)c(C(=O)N2C(C)CCCC2CNC(=O)c2cccc3cccnc23)s1
Reaction #89083
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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