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Cn1ccnc1

c1ccc(Cn2cnc3c(OC4CN5CCC4CC5)nccc32)cc1
Reaction #1010
title compound
Ausbeute 48.6%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCCC(O)(c2nc3c(Cl)nccc3n2Cc2ccccc2)C1
Reaction #1011
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1NCCn2cc(-c3ccccc3OC)nc21
Reaction #6863
desired product
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
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
CC1(c2ccc(C#N)cc2)C(=O)N(Cc2ccccc2)Cc2cncn21.Cl
Reaction #43694
4-(7-benzyl-5-methyl-6-oxo-5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazin-5-yl)-benzonitrile hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cc(NC(=O)OC(C)(C)C)ccc2n1CC(=O)O
Reaction #43811
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cc(N)ccc2n1CC(=O)OC(C)(C)C
Reaction #43812
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cc(NC(=O)OC(C)(C)C)ccc2n1CC(=O)OC(C)(C)C
Reaction #43854
crude sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #44417
semi-solid
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
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