An 21 Reaktionen beteiligt

440

CC(=O)Nc1cc(Nc2cc(NC3CC3)n3ncc(C#N)c3n2)ccc1C
Reaction #783
Ausbeute 18.1%750 AstraZeneca ELN dataset
CC(=O)Nc1cc(Nc2cc(NC3CC3)n3ncc(C#N)c3n2)ccc1C
Reaction #784
Ausbeute 18.6%750 AstraZeneca ELN dataset
CC(=O)Nc1cc(Nc2cc(NC3CC3)n3ncc(C#N)c3n2)ccc1C
Reaction #785
Ausbeute 22.6%750 AstraZeneca ELN dataset
CC(=O)Nc1cc(Nc2cc(NC3CC3)n3ncc(C#N)c3n2)ccc1C
Reaction #786
Ausbeute 0.0%750 AstraZeneca ELN dataset
CC(=O)Nc1cc(Nc2cc(Nc3cn(C)cn3)n3ncc(C#N)c3n2)ccc1C
Reaction #807
Ausbeute 12.8%750 AstraZeneca ELN dataset
CC(=O)Nc1cc(Nc2cc(Nc3cn(C)cn3)n3ncc(C#N)c3n2)ccc1C
Reaction #808
Ausbeute 29.3%750 AstraZeneca ELN dataset
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)ccc1C
Reaction #824
Ausbeute 16.5%750 AstraZeneca ELN dataset
CC(=O)Nc1cc(Nc2cc(Nc3ccn(C)n3)n3ncc(C#N)c3n2)ccc1C
Reaction #837
Ausbeute 33.2%750 AstraZeneca ELN dataset
COc1ccc(CN(c2ccc(OC)cn2)c2cc(Nc3ccc(C)c(NC(C)=O)c3)nn3c(C#N)cnc23)cc1
Reaction #249854
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(N)cc1Nc1ncc(-c2ccc(C#N)cc2)o1
Reaction #746922
title compound
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
Cc1ccc([N+](=O)[O-])cc1Nc1ncc(-c2ccc(C#N)cc2)o1
Reaction #746923
4-[2-(2-Methyl-5-nitro-phenylamino)-oxazol-5-yl]-benzonitrile
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
Cc1cccc(Cl)c1Nc1ncc(-c2ccc(C#N)cc2)o1
Reaction #746924
4-[2-(6-Chloro-2-methyl-phenylamino)-oxazol-5-yl]-benzonitrile
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
COc1cc(Nc2ncc(-c3ccc(C#N)cc3)o2)cc(OC)c1
Reaction #746925
4-[2-(3,5-Dimethoxy-phenylamino)-oxazol-5-yl]-benzonitrile
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
Cc1cccc(Nc2ncc(-c3ccc(C#N)cc3)o2)c1C
Reaction #746926
4-[2-(2,3-Dimethyl-phenylamino)-oxazol-5-yl]-benzonitrile
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
COC(=O)c1cnc(Nc2cc(N)ccc2C)o1
Reaction #746929
2-(5-Amino-2-methyl-phenylamino)-oxazole-5-carboxylic acid methyl ester
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
CC(=O)Nc1cc(N)ccc1C
Reaction #786593
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COc1ccc(CNC2CC2)cc1
Reaction #976633
Example 1
Ausbeute 100.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
COc1ccc(CN(c2ccc(OC)cn2)c2cc(Nc3ccc(C)c(NC(C)=O)c3)nn3c(C#N)cnc23)cc1
Reaction #976638
5C
Ausbeute 61.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CC(=O)Nc1cc(Nc2cc(Nc3cccc(C(=O)NCCN(C)C)c3)c3ncc(C#N)n3n2)ccc1C
Reaction #976656
3-(6-(3-Acetamido-4-methylphenylamino)-3-cyanoimidazo[1,2-b]pyridazin-8-ylamino)-N-(2-(dimethylamino)ethyl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
COc1ccc(CNC2CC2)cc1
Reaction #2293546
Example 1
Ausbeute 496.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_06
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