2-pyrrolidinone

CC(=O)c1cccc(N2CCCC2=O)c1
Reaction #44052
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1CCCN1c1cccc(CCO)c1
Reaction #44156
title compound
Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C/C=C(/C(=O)OC)N1CCCC1=O
Reaction #53758
product
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2cc(F)c(NC3=NCCC3)cc2n1Cc1ccccc1
Reaction #68427
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C1CCCN1c1ccc(Cl)cc1F
Reaction #68496
1-(4-chloro-2-fluorophenyl)pyrrolidin-2-one
Ausbeute 108.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C1CCCN1c1ccc(Cl)nc1
Reaction #70458
desired product
Ausbeute 103.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C/C=C(/C(=O)OC)N1CCCC1=O
Reaction #79504
product
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCCCCCCCCCCCN1CCCC1=O
Reaction #89801
N-dodecylpyrrolidin-2-one
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C1CCCN1c1ccc2c(c1)ncn2-c1cc(NS(=O)(=O)C2CC2)cc(-c2ccc(F)cc2F)c1
Reaction #92473
crude residue
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC1(C)Oc2ccc(C#N)cc2[C@@H](N2CCCC2=O)[C@@H]1O
Reaction #93186
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CC(=O)c1ccc2c(c1)[C@@H](N1CCCC1=O)[C@H](O)C(C)(C)O2
Reaction #93188
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
Cl.Cl.O=C1CCCN1c1ccc(OCCCN(CCn2ccc3ccccc3c2=O)Cc2ccncc2)cc1
Reaction #156194
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COCc1nn2c(CN3CC(CC(F)(F)Cl)CC3=O)c(C(F)(F)F)nc2s1
Reaction #156741
4-(2-chloro-2,2-difluoroethyl)-1-{[2-(methoxymethyl)-6-(trifluoromethyl)imidazo[2,1-b][1,3,4]thiadiazol-5-yl]methyl}pyrrolidin-2-one
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1nc(/C(=C/N2CCCC2=O)c2ccc(C(C)(C)C)cc2)ccc1Cl
Reaction #157882
1-[(E)-2-(4-tert-butylphenyl)-2-(5-chloro-6-methoxypyridin-2-yl)ethenyl]pyrrolidin-2-one
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1CCCN1Cc1ccc(I)cc1
Reaction #163337
1-(4-Iodobenzyl)pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1c(SCc2ccccc2)cccc1N1CCCC1=O
Reaction #163993
1-(3-Benzylsulfanyl-2-methyl-phenyl)-pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)C1(c2ccc(N3CCCC3=O)cc2)CC1
Reaction #174371
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(Nc1nc(Cl)cc(N2CCCC2=O)n1)c1ccc(F)cc1
Reaction #185378
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(OCC(=O)N1CCCC1=O)c1ccccc1
Reaction #185834
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1ccc(Oc2ccnc3cc(N4CCCC4=O)sc23)c(F)c1
Reaction #186489
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Seite 1Weiter