imidazolidine-2,4-dione

COc1cccc(C=C2NC(=O)NC2=O)c1OCc1ccccc1
Reaction #5992
5-[[3-Methoxy-2-(phenylmethoxy)phenyl]methylene]-2,4-imidazolidinedione
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(CN1C(=O)CNC1=O)OCc1ccccc1
Reaction #51839
phenylmethyl 2-(2,5-dioxoimidazolidinyl)acetate
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C1NC(=O)C(=Cc2ccccc2)N1
Reaction #95432
5-benzylidene hydantoin
Выход 91.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
O=C1NC(=O)C(=Cc2ccccc2)N1
Reaction #95433
5-benzylidene hydantoin
Выход 94.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
O=C1NC(=O)C(=Cc2ccc([N+](=O)[O-])cc2)N1
Reaction #95434
5-(4'-nitrobenzylidene)-hydantoin
Выход 93.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCCCCCCCCN1C(=O)CN(C)C1=O
Reaction #96069
1-methyl-3-n-nonyl hydantoin
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
O=C1NC(=O)C(=Cc2ccc([N+](=O)[O-])cc2)N1
Reaction #175499
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1CN(CP(=O)(O)O)C(=O)N1
Reaction #178570
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1CNC(=O)N1Cc1cccc(Br)c1
Reaction #192326
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc([N+](=O)[O-])c(C=C2NC(=O)NC2=O)c1
Reaction #197118
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1NC(=O)C(=Cc2cccnc2)N1
Reaction #207348
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1CNC(=O)N1CCCOCc1ccccc1
Reaction #207910
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C=C2NC(=O)NC2=O)cc1OCc1ccccc1
Reaction #209573
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(C=C2NC(=O)NC2=O)ccc1O
Reaction #215917
product
Выход 42.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
COc1cc(C=C2NC(=O)NC2=O)cc(OC)c1O
Reaction #215918
product
Выход 75.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CC(C)(C)c1cc(C=C2NC(=O)NC2=O)cc(C(C)(C)C)c1O
Reaction #215919
product
Выход 50.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CN1CC=C(c2c[nH]c3ccc(C=C4NC(=O)NC4=O)cc23)CC1
Reaction #216148
desired product
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CS(=O)(=O)c1ccc(C(CC2CCCC2)C(=O)Nc2cnc(C=C3NC(=O)NC3=O)cn2)cc1Cl
Reaction #221333
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc(C=C2NC(=O)NC2=O)cc(OC)c1O
Reaction #223669
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CSc1cc(NC2CC2)n2ncc(C=C3NC(=O)NC3=O)c2n1
Reaction #226685
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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