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Cc1cccnc1Cl

N#Cc1cnc(N)c(C#N)c1
Reaction #4542
2-Amino-3,5-dicyanopyridine
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
O=CCCn1cc(-c2cccnc2Cl)c(=O)[nH]c1=O
Reaction #40999
3-[5-(2-Chloro-pyridin-3-yl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-propionaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=c1[nH]c(=O)n(CCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1-c1cccnc1Cl
Reaction #41081
title compound
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cn(CCCN3C[C@@H]4C[C@]4(c4ccc(C(F)(F)F)cc4)C3)c(=O)[nH]c2=O)c(Cl)n1.Cl.Cl
Reaction #41084
title compound
Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cn(CCCN3C[C@@H]4C[C@]4(c4ccc(C(F)(F)F)cc4)C3)c(=O)[nH]c2=O)c(Cl)n1.Cl.Cl
Reaction #41085
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N)nc1Cl
Reaction #46226
6-chloro-5-methyl-pyridin-2-ylamine
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCc2c(Cl)cnc(Cl)c21
Reaction #49620
4,7-dichloro-1,2-dihydropyrrolo[3,4-c]pyridine-3-one
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCN(C(=O)c2cccnc2Cl)CC1
Reaction #58745
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)C2(c3ccc4c(c3)OC(F)(F)O4)CC2)nc1Cl
Reaction #67737
N-(6-chloro-5-methylpyridin-2-yl)-1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
NCc1cc(F)c(Cl)nc1Cl
Reaction #68413
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NCc1cncc(F)c1
Reaction #68414
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNc1ncccc1NC(=O)c1cc([N+](=O)[O-])cnc1Cl
Reaction #81813
2-Chloro-N-(2-ethylamino-3-pyridinyl)-5-nitro-3-pyridinecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCN1c2ncccc2NC(=O)c2cc([N+](=O)[O-])cnc21
Reaction #81814
title compound
Ausbeute 58.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-n2ccnc2)nc(Cl)c1C#N
Reaction #81830
title compound
Ausbeute 22.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-n2ccnc2)nc(Cl)c1C(N)=O
Reaction #81831
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(OC(F)(F)F)cc1)c1cnc(N2CC[C@@H](O)C2)c(-c2[nH]ncc2F)c1
Reaction #160921
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(OC(F)(F)F)cc1)c1cnc(Cl)c(-c2[nH]ncc2F)c1
Reaction #160922
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(OC(F)(F)Cl)cc1)c1cnc(N2CC[C@@H](O)C2)c(-c2[nH]ncc2F)c1
Reaction #160970
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(OC(F)(F)Cl)cc1)c1cnc(Cl)c(-c2[nH]ncc2F)c1
Reaction #160971
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(OC(F)(F)Cl)cc1)c1cnc(N2CC[C@H](O)C2)c(-c2[nH]ncc2F)c1
Reaction #160992
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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