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1164641

CS(=O)(=O)O.Cc1ccc(NC(=O)c2ccc(CN3CCN(C)CC3)c(C(F)(F)F)c2)cc1Nc1cc(-c2cccnc2)ccn1
Reaction #42065
objective compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc2c(-c3ccc(F)cc3)c(-c3ccnc(Nc4ccc(S(N)(=O)=O)cc4)c3)c(-c3ccc(F)cc3)nc2n1
Reaction #70888
desired compound
Ausbeute 17.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)c2ccc(CN3CCN(C)CC3)c(C(F)(F)F)c2)cc1Nc1cc(-c2cccnc2)ccn1
Reaction #174427
DOI: 10.1039/C8SC04228D
CCNC(=O)Nc1cc(-c2cncc(F)c2)c(-c2cncc(C(=O)O)c2)cn1
Reaction #177792
DOI: 10.1039/C8SC04228D
Cn1cc2c(-c3ccc(F)cc3)c(-c3ccnc(Nc4ccc(S(N)(=O)=O)cc4)c3)c(-c3ccc(F)cc3)nc2n1
Reaction #186918
DOI: 10.1039/C8SC04228D
CNc1cc(-c2cccnc2Oc2ccc(Nc3nnc(-c4ccccc4)c4c3CCC4)cc2)ccn1
Reaction #314962
N-(4-(3-(2-(methylamino)pyridin-4-yl)pyridin-2-yloxy)phenyl)-4-phenyl-6,7-dihydro-5H-cyclopenta[d]pyridazin-1-amine
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC[C@@H](COc2ccc(-c3c(C#N)c(N)nc(SCc4coc(-c5ccc(Cl)cc5)n4)c3C#N)cn2)O1
Reaction #329346
2′-Amino-6′-({[2-(4-chlorophenyl)-1,3-oxazol-4-yl]methyl}thio)-6-{[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]methoxy}-3,4′-bipyridine-3′,5′-dicarbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(N)nc(SCc2csc(Nc3ccc(F)c(Cl)c3)n2)c(C#N)c1-c1ccc(OCCO)nc1
Reaction #329351
2′-Amino-6′-[({2-[(3-chloro-4-fluorophenyl)amino]-1,3-thiazol-4-yl}methyl)thio]-6-(2-hydroxyethoxy)-3,4′-bipyridine-3′,5′-dicarbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(N)nc(SCc2csc(Nc3ccc(F)cc3)n2)c(C#N)c1-c1ccc(NCCO)nc1
Reaction #329352
2′-Amino-6′-[({2-[(4-fluorophenyl)amino]-1,3-thiazol-4-yl}methyl)thio]-6-[(2-hydroxyethyl)amino]-3,4′-bipyridine-3′,5′-dicarbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(N)nc(SCc2coc(-c3ccc(Cl)cc3)n2)c(C#N)c1-c1ccc(OC[C@@H](O)CO)nc1
Reaction #329356
2′-Amino-6′-({[2-(4-chlorophenyl)-1,3-oxazol-4-yl]methyl}thio)-6-{[(2S)-2,3-dihydroxypropyl]-oxy}-3,4′-bipyridine-3′,5′-dicarbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
COc1ncccc1-c1ccnc(N)c1
Reaction #337305
2-methoxy-3,4′-bipyridin-2′-amine
Ausbeute 93.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncccc1-c1ccnc(N=C=S)c1
Reaction #337306
2′-isothiocyanato-2-methoxy-3,4′-bipyridine
Ausbeute 72.2%DOI: 10.6084/m9.figshare.5104873.v1
CNc1cc(-c2cccnc2Oc2ccc(Nc3nnc(-c4ccccc4)c4c3CCC4)cc2)ccn1
Reaction #378304
DOI: 10.1039/C8SC04228D
COc1ccc2c3c(c(NCCN4CCCC4)nc2c1C)C(=O)c1ccncc1-3
Reaction #406545
DOI: 10.1039/C8SC04228D
Cn1cc(-c2ccnc(-n3ncc4cc(C(C)(C)C)cc(F)c4c3=O)c2CO)cc(Nc2ccc(C(=O)N3CCOCC3)cn2)c1=O
Reaction #424471
desired product
Ausbeute 81.8%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2ccnc(-n3ncc4cc(C(C)(C)C)cc(F)c4c3=O)c2CO)cc(Nc2ccc(S(C)(=O)=O)cn2)c1=O
Reaction #424472
desired product
Ausbeute 58.1%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2ccnc(-n3ncc4cc(C(C)(C)C)cc(F)c4c3=O)c2C=O)cc(Nc2ccc(N3CCN(C4COC4)CC3)cn2)c1=O
Reaction #494797
103c
Ausbeute 80.6%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2ccnc(-n3ncc4cc(C(C)(C)C)cc(F)c4c3=O)c2CO)cc(Nc2ccc(N3CCN(C4COC4)CC3)cn2)c1=O
Reaction #494798
103
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C2COC2)CCN1c1ccc(Nc2cc(-c3ccnc(-n4ncc5cc(C(C)(C)C)cc(F)c5c4=O)c3C=O)cn(C)c2=O)nc1
Reaction #494804
106b
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C2COC2)CCN1c1ccc(Nc2cc(-c3ccnc(-n4ncc5cc(C(C)(C)C)cc(F)c5c4=O)c3CO)cn(C)c2=O)nc1
Reaction #494805
106
Ausbeute 8.2%DOI: 10.6084/m9.figshare.5104873.v1
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