1,3-oxazolidin-2-one

N#Cc1ccc(-c2csc(N3CCOC3=O)n2)cc1
Reaction #173
Rendement 0.0%750 AstraZeneca ELN dataset
CCOC(=O)C1(C(=O)OCC)Oc2ccccc2O1
Reaction #5674
1,3-benzodioxole-2,2-dicarboxylic acid, diethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)c1cccc(N2CCOC2=O)c1
Reaction #44054
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1OCCN1c1cccc(CCO)c1
Reaction #44131
title compound
Rendement 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(Cn1c(C(=O)Nc2ccc(N3CCOC3=O)cc2)nc2ccccc21)Nc1ccc(Cl)cn1
Reaction #46814
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)SC[C@H]1CCCCCC[C@H](C(=O)N2C(=O)OC[C@H]2Cc2ccccc2)NC1=O
Reaction #50253
N-[[trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecan-10-yl]-carbonyl]-(R)-4-benzyl-2-oxazolidinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CCCC[C@@H](C)CCC(=O)N1C(=O)O[C@@H](c2ccccc2)[C@H]1C
Reaction #56711
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
C[C@@H](CC(=O)N1C(=O)OC[C@@H]1c1ccccc1)c1ccccc1
Reaction #61114
(S)-4-phenyl-3-((S)-3-phenyl-butyryl)-oxazolidin-2-one
Rendement 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C1OCCN1Cc1ccc([N+](=O)[O-])cc1
Reaction #72549
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C1OCCN1Cc1ccc([N+](=O)[O-])cc1F
Reaction #72581
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC[C@@H]1C(=O)N(C)c2cnc(-n3ccnc3N3CCOC3=O)nc2N1C1CCCC1
Reaction #73124
title compound
Rendement 6.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=Cc1c(F)cc(OC(=O)N2CCOC2=O)cc1F
Reaction #155419
3,5-difluoro-4-formylphenyl 2-oxooxazolidine-3-carboxylate
Rendement 98.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=Cc1ccc(OC(=O)N2CCOC2=O)cc1F
Reaction #155435
3-fluoro-4-formylphenyl 2-oxooxazolidine-3-carboxylate
Rendement 126.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(OC(=O)N2CCOC2=O)c(C=O)c1
Reaction #155436
2-formyl-4-methylphenyl 2-oxooxazolidine-3-carboxylate
Rendement 145.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1nc(/C(=C/CN2CCOC2=O)c2ccc(C(C)(C)C)cc2)ccc1Cl
Reaction #157880
3-[(2E)-3-(4-tert-butylphenyl)-3-(5-chloro-6-methoxypyridin-2-yl)prop-2-en-1-yl]-1,3-oxazolidin-2-one
Rendement 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC[C@H](CO)[C@@H](O[Si](C)(C)C)c1cccc(OCC2CCCCC2)c1
Reaction #161531
(R)-2-((R)-(3-(cyclohexylmethoxy)phenyl)-(trimethylsilyloxy)methyl)butan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cccc(N2CCNC2=O)c1
Reaction #173737
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(N2CCN(C(=O)c3ccc(N4CCOC4=O)cc3C)CC2)c(C)c1
Reaction #180079
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cn(-c2ccc(N3CCOC3=O)cc2F)nc(-c2ccnn2-c2ccccc2)c1=O
Reaction #186885
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(N2CCN(C(=O)c3ccc(N4CCOC4=O)cc3Cl)CC2)c(C)c1
Reaction #187658
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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