benzoxazinone

CCCCCCCCc1ccc2nc(Nc3cccc(Cl)c3)oc(=O)c2c1
Reaction #518131
2-(3-chlorophenylamino)-6-octyl-4H-3,1-benzoxazin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
CCCCCCCCc1ccc2nc(Nc3cccc(Cl)c3)oc(=O)c2c1
Reaction #589688
2-(3-chlorophenylamino)-6-octyl-4H-3,1-benzoxazin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
O=C1COc2ccc(CCc3cccc(F)c3)cc2N1
Reaction #657336
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CC(C)(C)c1ccc(-c2nc3ccc([N+](=O)[O-])cc3c(=O)o2)cc1
Reaction #929565
solid
Ausbeute 93.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
COC(=O)c1ccc(NC(=O)c2ccc(C(C)(C)C)cc2)c(C(=O)Nc2ccc(Cl)cn2)c1
Reaction #1075913
title compound
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_10
C1=Cc2ccccc2ON1
Reaction #1231417
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
COC(=O)c1ccc(NC(=O)c2ccc(C(C)(C)C)cc2)c(C(=O)Nc2ccc(Cl)cn2)c1
Reaction #1334361
title compound
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_10
Cc1cc(C#N)cc2c(=O)oc(-c3cc(Br)nn3-c3ncccc3Cl)nc12
Reaction #1383722
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_07
Cc1cc(Cl)cc(C(=O)NC(C)CSC[Si](C)(C)C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #1435694
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_05
N#Cc1cccc(C2Oc3ccccc3NC2=O)c1
Reaction #1722224
2-(3-Cyanophenyl)-3,4-dihydro-2H-1,4-benzoxazin-3-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_01
COC(=O)c1ccc(NC(=O)c2ccc(C(C)(C)C)cc2)c(C(=O)Nc2ccc(Cl)cn2)c1
Reaction #1970262
title compound
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_07
CC(C)(C)c1ccc(-c2nc3ccc([N+](=O)[O-])cc3c(=O)o2)cc1
Reaction #2389013
solid
Ausbeute 93.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_12
CCOC(=O)Nc1cccc(C)c1C(=O)O
Reaction #2438461
2-Ethoxycarbonylamino-6-methylbenzoic Acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_10