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768153

Cl.Cl.O=c1[nH]c2ncccc2n1C1CCNCC1
Reaction #42659
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #42660
title compound
Ausbeute 49.9%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=c1[nH]c2ncccc2n1C1CCNCC1
Reaction #48348
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #48349
title compound
Ausbeute 49.9%DOI: 10.6084/m9.figshare.5104873.v1
COCCN1C[C@H](c2ccccc2)CC[C@@H](NC(=O)N2CCC(n3c(=O)[nH]c4ncccc43)CC2)C1=O
Reaction #48432
title compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCC(c2ccc(O)cc2)CC[C@H]1NC(=O)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #48433
title compound
Ausbeute 33.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CO[C@@H](c2ccccc2)CN(CC2CC2)C1=O)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #48434
title compound
Ausbeute 85.8%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)CCN1C[C@H](c2cccc(F)c2F)CC[C@@H](NC(=O)N2CCC(n3c(=O)[nH]c4ncccc43)CC2)C1=O
Reaction #48436
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)CCN1C[C@H](c2cccc(F)c2F)CC[C@@H](NC(=O)N2CCC(n3c(=O)[nH]c4ncccc43)CC2)C1=O
Reaction #48437
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCN1C[C@H](c2cccc(F)c2F)CC[C@@H](NC(=O)N2CCC(n3c(=O)[nH]c4ncccc43)CC2)C1=O
Reaction #48438
title compound
Ausbeute 74.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CC[C@@H](c2cccc(F)c2F)CN(CC(F)(F)F)C1=O)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #48439
title compound
Ausbeute 62.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CC[C@@H](c2cccc(F)c2F)CN(Cc2ccccn2)C1=O)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #48440
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CC[C@@H](c2cccc(F)c2F)CN(c2ccncc2)C1=O)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #48441
title compound
Ausbeute 71.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CC[C@@H](c2cccc(F)c2F)CN(Cc2nccs2)C1=O)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #48442
title compound
Ausbeute 76.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)CN1C[C@H](c2cccc(F)c2F)CC[C@@H](NC(=O)N2CCC(n3c(=O)[nH]c4ncccc43)CC2)C1=O
Reaction #48443
title compound
Ausbeute 72.7%DOI: 10.6084/m9.figshare.5104873.v1
CCN1C[C@H](c2cccc(F)c2F)CC[C@@H](NC(=NC#N)N2CCC(n3c(=O)[nH]c4ncccc43)CC2)C1=O
Reaction #48446
title compound
Ausbeute 4.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(CO)[C@H](c2cccc(F)c2F)CC[C@H]1NC(=O)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #48451
title compound
Ausbeute 15.7%DOI: 10.6084/m9.figshare.5104873.v1
COCCN1CC(c2cccc(F)c2F)CC(NC(=O)N2CCC(n3c(=O)[nH]c4ncccc43)CC2)C1=O
Reaction #48454
title compound
Ausbeute 42.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CN(Cc2cccc(F)c2F)CCN(CC(F)(F)F)C1=O)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #48458
title compound
Ausbeute 86.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(N2CCC(n3c(=O)[nH]c4ncccc43)CC2)ncn1
Reaction #161687
ethyl 6-[4-(2-oxo-2,3-dihydro-imidazo[4,5-b]pyridin-1-yl)-piperidin-1-yl]-pyrimidine-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
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