3-oxo-4H-1,4-benzoxazine-6-carbaldehyde

Cl.O=C1COc2ccc(CNC3CCN(CC4Cn5c(=O)ccc6ncc(Cl)c4c65)CC3)cc2N1
Reaction #43599
title compound
Rendimiento 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc2ncc(=O)n(CCN3CCC(NCc4ccc5c(c4)NC(=O)CO5)CC3)c2c1
Reaction #68097
6-(((1-(2-(7-methoxy-2-oxoquinoxaline-1-(2H)-yl)ethyl)piperidin-4-yl)amino)methyl)-2H-1,4-benzooxazine-3(4H)-one
Rendimiento 19.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C1COc2ccc(CNC3CCC(C(=O)c4nc5ccccc5s4)CC3)cc2N1
Reaction #173029
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cl
Reaction #175057
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc2sc(OC3CCC(NCc4ccc5c(c4)NC(=O)CO5)CC3)nc12
Reaction #282766
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cl.O=C1COc2ccc(CNC3CCN(CCn4c(=O)ccc5cccnc54)CC3)cc2N1
Reaction #472814
6-(((1-(2-(2-oxo-1,8-naphthyridin-1(2H)-yl)ethyl)piperidin-4-yl)amino)methyl)-2H-1,4-benzoxazin-3(4H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
NS(=O)(=O)c1ccc(N2CCN(Cc3ccc4c(c3)NC(=O)CO4)CC2)cc1
Reaction #654057
4-[4-(3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethyl)-piperazin-1-yl]-benzenesulfonamide
Rendimiento 4.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
COc1ccc2ncc3c(c2n1)CC(C[C@H]1CC[C@H](NCc2ccc4c(c2)NC(=O)CO4)CC1)O3
Reaction #720994
6-{[trans-4-(8-methoxy-1,2-dihydro-3-oxa-5,9-diaza-cyclopenta[a]naphthalen-2-ylmethyl)-cyclohexylamino]-methyl}-4H-benzo[1,4]oxazin-3-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
CC(C)(C)OC(=O)N1CCN(Cc2ccc3c(c2)NC(=O)CO3)CC1
Reaction #916358
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=C1COc2ccc(CN[C@H]3CC[C@H](C(=O)c4nc5ccccc5s4)CC3)cc2N1
Reaction #1100095
title compound
Rendimiento 31.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
COc1ccc2nc(C(=O)[C@H]3CC[C@H](NCc4ccc5c(c4)NC(=O)CO5)CC3)sc2c1
Reaction #1100100
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
COc1cccc2sc(C(=O)[C@H]3CC[C@H](NCc4ccc5c(c4)NC(=O)CO5)CC3)nc12
Reaction #1100103
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
CCOc1cccc2sc(C(=O)[C@H]3CC[C@H](NCc4ccc5c(c4)NC(=O)CO5)CC3)nc12
Reaction #1100107
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
O=C1COc2ccc(CN[C@H]3CC[C@H](C(=O)c4cc5ccccc5s4)CC3)cc2N1
Reaction #1100112
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
COc1cccc2sc(O[C@H]3CC[C@H](NCc4ccc5c(c4)NC(=O)CO5)CC3)nc12
Reaction #1100118
title compound
Rendimiento 16.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
O=C1COc2ccccc2N1
Reaction #1107103
4H-benzo[1,4]oxazin-3-one
Rendimiento 167.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
CN1C(=O)COc2ccc(C=O)cc21
Reaction #1132544
4-methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-6-carbaldehyde
Rendimiento 85.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
COc1ccc2nccc(C(O)CN3CCCC(CNCc4ccc5c(c4)NC(=O)CO5)C3)c2c1
Reaction #1230771
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
NS(=O)(=O)c1ccc(N2CCN(Cc3ccc4c(c3)NC(=O)CO4)CC2)cc1
Reaction #1309415
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CN1C(=O)COc2ccc(C=O)cc21
Reaction #1314485
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
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