Recherche de Sous-structure

N=CN

CSC1=N[C@@H](c2ccccc2)[C@@H](c2ccccc2)N1.I
Reaction #46990
product 42
Rendement 98.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@H](c2ccccc2)[C@@H](c2ccccc2)N1
Reaction #47002
product 122
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C)c(C)c(CSC2=N[C@@H](c3ccccc3)[C@@H](c3ccccc3)N2)c(C)c1C.Cl
Reaction #47063
product 234
Rendement 52.5%DOI: 10.6084/m9.figshare.5104873.v1
CSC1=N[C@@H](c2ccccc2)[C@@H](c2ccccc2)N1C(=O)Oc1ccccc1
Reaction #47117
product 548
Rendement 59.2%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])N=C1NCCN1Cc1ccc(F)nc1
Reaction #50489
1-(2-fluoro-5-pyridylmethyl)-2-(nitroimino)imidazolidine
Rendement 50.2%DOI: 10.6084/m9.figshare.5104873.v1
COCC(=O)Nc1cccc([C@@]2(c3ccc(OC(F)F)cc3)N=C(N)N(C)C2=O)c1
Reaction #58838
N-(3-{(4R)-2-Amino-4-[4-(difluoromethoxy)phenyl]-1-methyl-5-oxo-4,5-dihydro-1H-imidazol-4-yl}phenyl)-2-methoxyacetamide
DOI: 10.6084/m9.figshare.5104873.v1
COCC1CC1c1cccc(C2(c3ccc(OC(F)F)cc3)N=C(N)N(C)C2=O)c1
Reaction #58864
title compound
Rendement 16.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)C(c2ccc(OC(F)F)cc2)(c2cccc(O)c2)N=C1N
Reaction #58869
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)C(c2ccc(OC(F)F)cc2)(c2cccc(C3CC(O)C3)c2)N=C1N
Reaction #58875
title compound
Rendement 94.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #77549
solid
Rendement 72.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #77550
solid
Rendement 45.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1OC[C@]2(c3cc(-c4cncc(C(F)(F)F)c4)ccc3F)N=C(N)SC[C@H]12
Reaction #155550
title compound
Rendement 25.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1=N[C@@]2(c3ccc(F)cc3F)CO[C@H](CO)[C@H]2CS1)c1ccccc1
Reaction #155557
title compound
Rendement 89.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1=N[C@@]2(c3ccc(F)cc3F)CO[C@H](CF)[C@H]2CS1)c1ccccc1
Reaction #155558
title compound
Rendement 65.6%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(c3ccc(F)cc3F)CO[C@H](CF)[C@H]2CS1
Reaction #155559
title compound
Rendement 104.2%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(c3cc(Br)c(F)cc3F)CO[C@H](CF)[C@H]2CS1
Reaction #155560
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1=N[C@@]2(c3cc(Br)c(F)cc3F)CO[C@H](CF)[C@H]2CS1
Reaction #155561
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(c3cc(-c4cncnc4)c(F)cc3F)CO[C@H](CF)[C@H]2CS1
Reaction #155562
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1OC[C@]2(c3ccc(F)cc3F)N=C(NC(=O)c3ccccc3)SC[C@H]12
Reaction #155566
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1OC[C@]2(c3cc(Br)c(F)cc3F)N=C(NC(=O)c3ccccc3)SC[C@H]12
Reaction #155567
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
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