#5944499

CC(=O)c1ccc(Oc2ccc3c(c2)S(=O)(=O)NC2CCCN32)cc1
Reaction #58055
1-{4-[(5,5-Dioxido-2,3,3a,4-tetrahydro-1H-pyrrolo[2,1-c][1,2,4]benzothiadiazin-7-yl)oxy]phenyl}ethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1ccc(-c2ccc(C(C)=O)cc2)cc1
Reaction #159267
4′-Methoxy-4-acetylbiphenyl
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1
Reaction #159268
4′-nitro-4-acetylbiphenyl
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1cc2nccc(Oc3ccc(C)nc3-c3ccc(C(C)=O)cc3)c2cc1OC
Reaction #178844
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)c1ccc(-c2c(-c3ccc(Cl)cc3)ccn3c(=O)n(Cc4ccc(C(F)(F)F)nc4)nc23)cc1
Reaction #181594
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ncc(F)cc1-c1ccc(C(C)=O)cc1
Reaction #190373
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)c1ccc(-c2ccc3cc[nH]c3c2)cc1
Reaction #199346
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOc1ncc(Cl)cc1-c1ccc(C(C)=O)cc1
Reaction #209045
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)c1ccc(-c2cnc3c(c2)N(Cc2ccccc2)C(=O)CN3)cc1
Reaction #229291
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)c1ccc(-c2ccc3c(c2)C(C)(C)CC3=O)cc1
Reaction #235007
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)c1ccc(-c2ccc(-n3c(CC4CCN(C(=O)C5CC5)C4)n[nH]c3=O)c(F)c2)cc1
Reaction #240135
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc2c(-c3ccc(C(C)=O)cc3)nc(Nc3cc[nH]n3)cc2c1
Reaction #253422
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)c1ccc(-c2ccc(-c3nc(CCN4CCCC4C)c(C)o3)cc2)cc1
Reaction #263028
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=O)c1ccc(-n2cc(C#N)c(Nc3ccc(S(C)(=O)=O)cc3)n2)cc1
Reaction #263729
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=O)c1ccc(-c2sc(N=C(c3ccccc3)c3ccccc3)nc2C)cc1
Reaction #278619
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccc(-c2nc3cc(-c4ccc(C(C)=O)cc4)ccc3o2)cc1[N+](=O)[O-]
Reaction #281926
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccc(CCNc2cc(-c3ccc(C(C)=O)cc3)nc(OC)n2)cc1
Reaction #289048
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=O)c1ccc(-c2cc(C(N)=O)c([N+](=O)[O-])s2)cc1
Reaction #294502
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCC(NC(c1ccc(-c2ccc(C(C)=O)cc2)cc1)C(F)(F)F)C(=O)NC1(C#N)CC1
Reaction #296986
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=O)c1ccc(-c2nccnc2N2CCN(Cc3cnn(C)c3C)CC2)cc1
Reaction #307747
1-{4-[4-(1,5-dimethyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl-3′-yl]-phenyl}-ethanone
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
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