6-bromo-3,4-dihydro-1H-1,8-naphthyridin-2-one

CC(C)(C)OC(=O)/C=C/c1cnc2c(c1)CCC(=O)N2
Reaction #46535
title compound
المردود 45.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)/C=C/c1cnc2c(c1)CCC(=O)N2
Reaction #46592
title compound
المردود 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(Cc1c[nH]c2ccccc12)C(=O)/C=C/c1cnc2c(c1)CCC(=O)N2
Reaction #46596
title compound
المردود 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(Cc1cn(Cc2ccccc2)c2ccccc12)C(=O)/C=C/c1cnc2c(c1)CCC(=O)N2
Reaction #46597
title compound
المردود 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)CCn1cc(CN(C)C(=O)/C=C/c2cnc3c(c2)CCC(=O)N3)c2ccccc21
Reaction #46598
title compound
المردود 17.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cccc2c(CN(C)C(=O)/C=C/c3cnc4c(c3)CCC(=O)N4)c(C)n(C)c12
Reaction #46610
title compound
المردود 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1CCc2cc(/C=C/C(=O)N3CCC3)cnc2N1
Reaction #170090
title compound
المردود 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1c(CN(C)C(=O)C=Cc2cnc3c(c2)CCC(=O)N3)n(C)c2ccccc12
Reaction #193707
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(CN(C)C(=O)C=Cc2cnc3c(c2)CCC(=O)N3)c1OCC(C)C
Reaction #201916
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(C)CCn1cc(CN(C)C(=O)C=Cc2cnc3c(c2)CCC(=O)N3)c2ccccc21
Reaction #204682
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)C=Cc1cnc2c(c1)CCC(=O)N2
Reaction #299399
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC1=C(CN(C)C(=O)/C=C/c2cnc3c(c2)CCC(=O)N3)Cc2ccccc21
Reaction #313106
title compound
المردود 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Cc1c(CN(C)C(=O)/C=C/c2cnc3c(c2)CCC(=O)N3)n(C)c2ccccc12
Reaction #313121
title compound
المردود 59.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CN(Cc1c[nH]c2ccccc12)C(=O)C=Cc1cnc2c(c1)CCC(=O)N2
Reaction #384501
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1cc(C)c(CNC(=O)c2cc(C3=CNC4=NC(=O)CCC4=C3)nc3c2cnn3C(C)C)c(=O)[nH]1
Reaction #563206
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
O=C1CCc2cc(/C=C/C(=O)N3CCC3)cnc2N1
Reaction #721046
title compound
المردود 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
CCn1ccc2c(CN(C)C(=O)C=Cc3cnc4c(c3)CCC(=O)N4)cccc21
Reaction #763358
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Cc1cccc2c(CN(C)C(=O)C=Cc3cnc4c(c3)CCC(=O)N4)c(C)n(C)c12
Reaction #765751
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Brc1cnc2c(c1)CCCN2
Reaction #799767
title compound
المردود 99.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CN(Cc1cn(Cc2ccccc2)c2ccccc12)C(=O)C=Cc1cnc2c(c1)CCC(=O)N2
Reaction #1201312
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
الصفحة 1التالي