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7228

CN1CCN(CCCNc2ncc3cc(-c4c(Cl)cccc4Cl)c(NC(=O)Nc4ccccc4)nc3n2)CC1
Reaction #3533
title compound
Выход 65.5%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCCCNc1ncc2cc(-c3c(Cl)cccc3Cl)c(NC(=O)Nc3ccccc3)nc2n1
Reaction #3535
title compound
Выход 66.4%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)Nc1nc2nc(NCCCCN(CC)CC)ncc2cc1-c1c(Cl)cccc1Cl.Cl
Reaction #3536
hydrochloric acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CN(C(=O)CCl)c1nc(-c2ccccc2Cl)c(-c2ccc(Cl)cc2)cc1C#N
Reaction #42114
2-chloro-N-(6-(2-chlorophenyl)-5-(4-chlorophenyl)-3-cyanopyridin-2-yl)-N-isobutylacetamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(=O)[nH]c1Nc1ccc(Br)cc1F
Reaction #44222
pure desired product
Выход 83.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(=O)[nH]c1Nc1ccc(Br)cc1F
Reaction #44223
pure desired product
Выход 93.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Oc2ccnc3c2CCN3)c(F)c1
Reaction #44702
[4-(2,3-Dihydro-1H-pyrrolo[2,3-b]pyridin-4-yloxy)-3-fluorophenyl]amine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(Nc2ccc(Oc3ccnc4c3CCN4)c(F)c2)cc(-c2ccncc2)n1
Reaction #44726
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(Nc2ccc(Oc3ccnc4c3CCN4)c(F)c2)cc(-c2ccc(F)cc2)n1
Reaction #44727
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc2c(nc1N)CCN(Cc1ccccc1)C2
Reaction #49975
2-amino-6-benzyl-5,6,7,8-tetrahydro-1,6-naphthyridine-3-carbonitrile
Выход 49.5%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc2c(nc1N)CCN(Cc1ccccc1)C2
Reaction #49978
2-amino-6-benzyl-5,6,7,8-tetrahydro-1,6-naphthyridine-3-carbonitrile
Выход 49.5%DOI: 10.6084/m9.figshare.5104873.v1
CCNc1ncccc1C(=O)Nc1c(C)ccnc1Cl
Reaction #81798
title compound
Выход 76.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(F)cnc1N1CC(Nc2ccc(F)cc2C)C1
Reaction #159632
title compound ( D90 )
Выход 44.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)ccc1NC1CN(c2ncc(F)cc2C(=O)O)C1
Reaction #159666
title compound ( D135 )
Выход 97.4%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #170183
solid
Выход 78.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1cc(F)c(N[C@@H]2CCCC[C@@H]2N)nc1Nc1cccnc1
Reaction #172045
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cccnc1Nc1cc(Cl)cc(Cl)c1
Reaction #178675
DOI: 10.1039/C8SC04228D
CC(=O)Nc1cnc(N2CCN(C(=O)OCc3ccccc3)CC2)c(C(F)(F)F)c1
Reaction #179790
DOI: 10.1039/C8SC04228D
Nc1ncc(-c2cnn(CC(=O)N3CCOCC3)c2)cc1-c1nc2ccccc2s1
Reaction #186034
DOI: 10.1039/C8SC04228D
COC(=O)c1cccnc1Nc1ccc(-c2cccc(O)c2)cc1F
Reaction #186834
DOI: 10.1039/C8SC04228D
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