N-[4-(3-formyl-2-hydroxy-1H-indole-6-carbonyl)phenyl]thiophene-2-carboxamide

COc1ccc(NC=C2C(=O)Nc3cc(C(=O)c4ccc(NC(=O)c5cccs5)cc4)ccc32)cc1O
Reaction #385998
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C1Nc2cc(C(=O)c3ccc(NC(=O)c4cccs4)cc3)ccc2C1=CNc1ccc(N2CCOCC2)cc1
Reaction #728036
title compound
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
O=C1Nc2cc(C(=O)c3ccc(NC(=O)c4cccs4)cc3)ccc2C1=CO
Reaction #728038
Thiophene-2-carboxylic acid [4-(3-hydroxymethylene-2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide
Ausbeute 75.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
CN1CCN(c2ccc(NC=C3C(=O)Nc4cc(C(=O)c5ccc(NC(=O)c6cccs6)cc5)ccc43)cc2)CC1
Reaction #728039
title compound
Ausbeute 59.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
O=C1Nc2cc(C(=O)c3ccc(NC(=O)c4cccs4)cc3)ccc2C1=CNc1cccc(O)c1
Reaction #728040
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
Cc1ccc(NC=C2C(=O)Nc3cc(C(=O)c4ccc(NC(=O)c5cccs5)cc4)ccc32)cc1O
Reaction #728041
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
COc1ccc(NC=C2C(=O)Nc3cc(C(=O)c4ccc(NC(=O)c5cccs5)cc4)ccc32)cc1O
Reaction #728042
title compound
Ausbeute 57.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
O=C1Nc2cc(C(=O)c3ccc(NC(=O)c4cccs4)cc3)ccc2C1=CNc1cccc(O)c1
Reaction #1201053
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CN1CCN(c2ccc(NC=C3C(=O)Nc4cc(C(=O)c5ccc(NC(=O)c6cccs6)cc5)ccc43)cc2)CC1
Reaction #1234503
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
Cc1ccc(NC=C2C(=O)Nc3cc(C(=O)c4ccc(NC(=O)c5cccs5)cc4)ccc32)cc1O
Reaction #1234821
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
O=C1Nc2cc(C(=O)c3ccc(NC(=O)c4cccs4)cc3)ccc2C1=CNc1ccc(N2CCOCC2)cc1
Reaction #1288672
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
O=C1Nc2cc(C(=O)c3ccc(NC(=O)c4cccs4)cc3)ccc2C1=CO
Reaction #2242271
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
O=C1Nc2cc(C(=O)c3ccc(NC(=O)c4cccs4)cc3)ccc2C1=CNc1ccc(N2CCOCC2)cc1
Reaction #2439973
title compound
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_07
O=C1Nc2cc(C(=O)c3ccc(NC(=O)c4cccs4)cc3)ccc2C1=CO
Reaction #2439975
Thiophene-2-carboxylic acid [4-(3-hydroxymethylene-2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide
Ausbeute 75.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_07
CN1CCN(c2ccc(NC=C3C(=O)Nc4cc(C(=O)c5ccc(NC(=O)c6cccs6)cc5)ccc43)cc2)CC1
Reaction #2439976
title compound
Ausbeute 59.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_07
O=C1Nc2cc(C(=O)c3ccc(NC(=O)c4cccs4)cc3)ccc2C1=CNc1cccc(O)c1
Reaction #2439977
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_07
Cc1ccc(NC=C2C(=O)Nc3cc(C(=O)c4ccc(NC(=O)c5cccs5)cc4)ccc32)cc1O
Reaction #2439978
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_07
COc1ccc(NC=C2C(=O)Nc3cc(C(=O)c4ccc(NC(=O)c5cccs5)cc4)ccc32)cc1O
Reaction #2439979
title compound
Ausbeute 57.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_07