5-Bromoindoline

NC(=O)c1ccccc1N1CCc2cc(Br)ccc21
Reaction #4102
2-(5-bromo-indolin-1-yl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=[N+]([O-])c1ccccc1N1CCc2cc(Br)ccc21
Reaction #4118
product
Rendimiento 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
NC(=O)c1ccccc1N1CCc2cc(Br)ccc21
Reaction #4160
2-(5-bromo-indolin-1-yl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=[N+]([O-])c1ccccc1N1CCc2cc(Br)ccc21
Reaction #4176
product
Rendimiento 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
NC(=O)c1ccccc1N1CCc2cc(Br)ccc21
Reaction #62598
2-(5-bromo-indolin-1-yl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
NC(=O)c1ccccc1N1CCc2cc(Br)ccc21
Reaction #62631
2-(5-bromo-indolin-1-yl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
O=[N+]([O-])c1ccccc1N1CCc2cc(Br)ccc21
Reaction #62648
product
Rendimiento 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
NC(=O)c1ccccc1N1CCc2cc(Br)ccc21
Reaction #63388
2-(5-bromo-indolin-1-yl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
O=[N+]([O-])c1ccccc1N1CCc2cc(Br)ccc21
Reaction #63404
5-Bromo-1-(2-nitrophenyl)indoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CC(C)(C)OC(=O)N1CCc2cc(Br)ccc21
Reaction #77782
5-Bromo-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester
Rendimiento 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)(C)c1ccc(CN2CCc3cc(-c4cn[nH]c4)ccc32)cc1
Reaction #91571
1-(4-(tert-butyl)benzyl)-5-(1H-pyrazol-4-yl)indoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=[N+]([O-])c1cc2c(cc1Br)CCN2
Reaction #161143
5-bromo-6-nitro-2,3-dihydro-1H-indole
Rendimiento 76.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(Nc1ccc(OCc2ccccn2)nc1)N1CCc2cc(Br)ccc21
Reaction #222425
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCS(=O)(=O)N1CCc2cc(Br)ccc21
Reaction #224834
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)S(=O)(=O)N1CCc2cc(Br)ccc21
Reaction #227175
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(Cc1ccccc1)N1CCc2cc(Br)ccc21
Reaction #249732
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NC(=S)N1CCc2cc(Br)ccc21
Reaction #256880
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=[N+]([O-])c1ccccc1N1CCc2cc(Br)ccc21
Reaction #261330
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)N1CCC(Oc2cc(N3CCc4cc(Br)ccc43)ncn2)CC1
Reaction #272032
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Brc1ccc2c(c1)CCN2CCN1CCCC1
Reaction #283881
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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