5-bromo-1,3-dihydropyrrolo[2,3-b]pyridin-2-one

O=C1Cc2cc(Br)cnc2N1
Reaction #46518
title compound
収率 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)/C=C/c1ccc2c(c1)CC(=O)N2
Reaction #46519
title compound
収率 162.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(-c2cnc3c(c2)CC(=O)N3)cc(OC)c1OC
Reaction #172226
compound
収率 30.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1Cc2cc(Br)cnc2N1
Reaction #190182
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c(C=C2C(=O)Nc3ncc(Br)cc32)[nH]c2c1C(=O)N(CCN1CCCCC1)CC2
Reaction #226346
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C1Cc2cc(-c3ccccc3)cnc2N1
Reaction #273870
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)c1cnc2c(c1)CC(=O)N2
Reaction #376470
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCN(CC)CCN1CCCc2[nH]c(C=C3C(=O)Nc4ncc(Br)cc43)c(C)c2C1=O
Reaction #378968
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1cc(-c2cnc3c(c2)CC(=O)N3)cc(OC)c1OC
Reaction #420350
compound
収率 30.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CN1C(=O)C(C)(C)c2cc(Br)cnc21
Reaction #532953
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=C1Nc2ncc(Br)cc2C1=Cc1ccc2cn[nH]c2c1
Reaction #534472
title compound
収率 146.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=C1Nc2ncc(Br)cc2C1=Cc1ccc2cn[nH]c2c1
Reaction #534618
title compound
収率 146.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=C1Cc2cc(Br)cnc2N1
Reaction #580327
4
収率 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
O=C1Cc2cc(-c3cccc(F)c3)cnc2N1
Reaction #580328
brown semisolid
収率 150.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
COc1cc(-c2cnc3c(c2)CC(=O)N3)cc(OC)c1OC
Reaction #799742
compound
収率 30.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
O=C1Cc2cc(Br)cnc2N1
Reaction #928101
5-bromo-7-azaoxindole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
O=C1Cc2cc(-c3ccccc3)cnc2N1
Reaction #928102
5-phenyl-7-azaoxindole
収率 51.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
O=C1Cc2cc(-c3ccco3)cnc2N1
Reaction #928103
solid
収率 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
CCOC(=O)c1cnc2c(c1)CC(=O)N2
Reaction #928104
5-(carboethoxy)-7-azaoxindole
収率 25.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
O=C1Cc2cc(Br)cnc2N1
Reaction #928118
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
1 ページ次のページ