An 94 Reaktionen beteiligt

950855

COC(=O)c1ccc(OCC2CC(Oc3ccc4ccccc4c3)CN2C(=O)Cc2ccc(NC(=O)Nc3ccccc3C)c(OC)c2)cc1
Reaction #185711
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(OCC2(C)CCCN2C(=O)Cc2ccc(NC(=O)Nc3ccccc3C)c(OC)c2)c([N+](=O)[O-])c1
Reaction #189879
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(OCC2CC(OC)CN2C(=O)Cc2ccc(NC(=O)Nc3ccccc3C)c(OC)c2)cc1
Reaction #206550
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(CC(=O)O)ccc1NC(=O)Nc1ccccc1C
Reaction #207893
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1ccc(OCC2CCCN2C(=O)Cc2ccc(NC(=O)Nc3ccccc3C)c(OC)c2)c(OC)c1
Reaction #251261
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)c1ccc(OCC2CCCN2C(=O)Cc2ccc(NC(=O)Nc3ccccc3C)c(OC)c2)c(OC)c1
Reaction #260806
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C1CN(C(=O)c2ccccc2)CC1c1ccc(NC(=O)Cc2ccc(NC(=O)Nc3ccccc3C)c(OC)c2)cc1
Reaction #280838
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)c1ccc(C#CC2CCCN2C(=O)Cc2ccc(NC(=O)Nc3ccccc3C)c(OC)c2)cc1
Reaction #281575
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)c1ccc(NCC2CCCN2C(=O)Cc2ccc(NC(=O)Nc3ccccc3C)c(OC)c2)cn1
Reaction #282588
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc(CC(=O)Nc2ccc(I)cc2)ccc1NC(=O)Nc1ccccc1C
Reaction #300486
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc(CC(=O)N(C)CC(=O)O)ccc1NC(=O)Nc1ccccc1C
Reaction #363069
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
COc1cc(CC(=O)NCC(=O)O)ccc1NC(=O)Nc1ccccc1C
Reaction #363071
title compound
Ausbeute 64.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
COc1cc(CC(=O)O)ccc1NC(=O)Nc1ccccc1C
Reaction #363073
title compound
Ausbeute 84.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CCOC(=O)c1ccc(C#CC2CCCN2C(=O)Cc2ccc(NC(=O)Nc3ccccc3C)c(OC)c2)cc1
Reaction #437522
ethyl 4-[2-[1-[3-methoxy-4-(N′-(2-methylphenyl)ureido]phenylacetyl]-2-pyrrolidinyl]ethynyl]benzoate
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
COc1cc(CC(=O)Oc2c(F)c(F)c(F)c(F)c2F)ccc1NC(=O)Nc1ccccc1C
Reaction #437527
pentafluorophenyl 3-methoxy-4-[N′-(2-methylphenyl) ureido]phenylacetate
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
COC(=O)c1ccc(OC[C@@H]2CCCN2C(=O)Cc2ccc(NC(=O)Nc3ccccc3C)c(OC)c2)cc1
Reaction #437531
methyl (S)-4-[1-[3-methoxy-4-[N′-(2-methylphenyl)ureido]phenylacetyl]-2-pyrrolidinylmethoxy]benzoate
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
CCOC(=O)c1ccc(OC[C@@H]2CCCN2C(=O)Cc2ccc(NC(=O)Nc3ccccc3C)c(OC)c2)c(OC)c1
Reaction #437533
ethyl (S)-3-methoxy-4-[1-[3-methoxy-4-[N′-(2-methylphenyl)ureido]phenyl acetyl]-2-pyrrolidinyl methoxy]benzoate
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
COC(=O)c1ccc(OC[C@@H]2CCCN2C(=O)Cc2ccc(NC(=O)Nc3ccccc3C)c(OC)c2)cc1C(=O)OC
Reaction #437535
dimethyl (S)-4-[1-[3-methoxy-4-[N′-(2-methylphenyl)ureido]phenylacetyl]-2-pyrrolidinylmethoxy]phthalate
Ausbeute 97.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
COC(=O)c1ccc(OC[C@@H]2CCCN2C(=O)Cc2ccc(NC(=O)Nc3ccccc3C)c(OC)c2)c(C(=O)OC)c1
Reaction #437546
dimethyl (S)-4-[1-[3-methoxy-4-[N′-(2-methylphenyl)ureido]phenylacetyl]-2-pyrrolidinylmethoxy]isophthalate
Ausbeute 115.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
COC(=O)c1ccc(OCC2(C)CCCN2C(=O)Cc2ccc(NC(=O)Nc3ccccc3C)c(OC)c2)c([N+](=O)[O-])c1
Reaction #437563
methyl 4-[[1-[3-methoxy4-[N′-(2-methylphenyl)ureido]phenylacetyl]-2-methyl-2-pyrrolidinyl]methoxy]-3-nitrobenzoate
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
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