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8946

CCc1cc(OCc2ccc(-c3ccccc3C#N)cc2)c2ccccc2n1
Reaction #5776
4'-[(2-ethylquinolin-4-yloxy)methyl]biphenyl-2-carbonitrile
Ausbeute 91.1%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(OCc2ccc(-c3ccccc3C#N)cc2)c2c(n1)CCCC2
Reaction #5777
4-[(2'-cyanobiphenyl-4-yl)methoxy]-2-ethyl-5,6,7,8-tetrahydroquinoline
Ausbeute 49.4%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(OCc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)c2ccccc2n1.Cl
Reaction #5778
2-ethyl-4-[(2'-(1H-tetrazol-5-yl)biphenyl-4-yl)methoxy]-quinoline hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)c1ccccc1-c1ccc(C(=O)Nc2ccccc2C(=O)Nc2ccc(Cl)cn2)cc1
Reaction #40410
2-[4-(N-{2-[N-(5-chloro-2-pyridyl)carbamoyl]phenyl}carbamoyl)phenyl]benzenecarboxamidine
Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1C(=O)Nc1ccc(Cl)cn1)c1ccc(-c2ccccc2C=NNO)cc1
Reaction #40411
N-{2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}{4-[2-((hydroxyamino)iminomethyl)phenyl]phenyl}carboxamide
Ausbeute 27.5%DOI: 10.6084/m9.figshare.5104873.v1
NCc1ccccc1-c1ccc(C(=O)Nc2ccccc2C(=O)Nc2ccc(Cl)cn2)cc1
Reaction #40412
{4-[2-(aminomethyl)phenyl]phenyl)-N-(2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}carboxamide
Ausbeute 43.1%DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)c1ccccc1-c1ccc(C(=O)Nc2ccccc2C(=O)Nc2ccc(Cl)cn2)cc1
Reaction #40439
2-[4-(N-{2-[N-(5-chloro-2-pyridyl)carbamoyl]phenyl}carbamoyl)phenyl]benzenecarboxamidine
Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1C(=O)Nc1ccc(Cl)cn1)c1ccc(-c2ccccc2C=NNO)cc1
Reaction #40440
N-{2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}{4-[2-((hydroxyamino)iminomethyl)phenyl]phenyl}carboxamide
Ausbeute 27.5%DOI: 10.6084/m9.figshare.5104873.v1
NCc1ccccc1-c1ccc(C(=O)Nc2ccccc2C(=O)Nc2ccc(Cl)cn2)cc1
Reaction #40441
{4-[2-(aminomethyl)phenyl]phenyl}-N-{2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}carboxamide
Ausbeute 43.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(C(C)C(=O)OC)c(=O)n1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #64495
desired material
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc(C)n(-c2ccccc2)c(=O)c1Cc1ccc(-c2ccccc2C#N)cc1F
Reaction #173804
DOI: 10.1039/C8SC04228D
CCc1cc2c(=O)n(CC(=O)C3CCCCC3)c(=O)n(Cc3ccc(-c4ccccc4C#N)cc3)c2s1
Reaction #184090
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cn(C)nc1NCc1ccc(-c2ccccc2C#N)cc1
Reaction #185779
DOI: 10.1039/C8SC04228D
CCc1cc2c(=O)n(CC(=O)c3cc(OC)cc(OC)c3)c(=O)n(Cc3ccc(-c4ccccc4C#N)cc3)c2s1
Reaction #188899
DOI: 10.1039/C8SC04228D
CCc1cc2c(=O)n(C(C)C(=O)OC)c(=O)n(Cc3ccc(-c4ccccc4C#N)cc3)c2s1
Reaction #189032
DOI: 10.1039/C8SC04228D
Cc1cc(OCc2ccc(-c3ccccc3C#N)cc2)cc(C)n1
Reaction #189760
DOI: 10.1039/C8SC04228D
CC(=O)OCc1ccc(-c2ccccc2C#N)cc1Br
Reaction #190206
DOI: 10.1039/C8SC04228D
CCc1cc2c(=O)n(CC(=O)c3ccc(OC)c(F)c3)c(=O)n(Cc3ccc(-c4ccccc4C#N)cc3F)c2s1
Reaction #190602
DOI: 10.1039/C8SC04228D
CCc1cc2c(=O)n(C(C)C(O)c3ccc(OC)cc3)c(=O)n(Cc3ccc(-c4ccccc4C#N)cc3)c2s1
Reaction #194724
DOI: 10.1039/C8SC04228D
CCCCc1nc(C)n(Cc2ccc(OC)nc2)c(=O)c1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #197467
DOI: 10.1039/C8SC04228D
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