1-chloro-3,3-dimethyl-2-butanone

CC(C)(C)C(=O)c1cc2cc(-c3ccc(Cl)cc3)c(-c3ccccc3Cl)nc2o1
Reaction #8910
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)C(=O)CC1C(=O)N(N)c2ccccc2-c2ccccc21.Cl
Reaction #51414
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(C)(C)OC(=O)NN1C(=O)C(CC(=O)C(C)(C)C)c2ccccc2-c2ccccc21
Reaction #220426
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
Cc1cc([N+](=O)[O-])ccc1N=C1SCC(CC(C)C)N1CC(=O)C(C)(C)C
Reaction #223644
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)C(=O)CN1CCNC1=N[N+](=O)[O-]
Reaction #258172
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)C(=O)COc1ccc(Cl)cc1
Reaction #261762
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCn1c(C(=O)N(C2CC2)C2CC2)cc2c3c(ncn3C)c(Nc3nc(C(C)(C)C)cs3)nc21
Reaction #307535
4-(4-tert-butylthiazol-2-ylamino)-N,N-dicyclopropyl-6-ethyl-1-methyl-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(=O)N1CCC(c2ccc(OCC(=O)C(C)(C)C)c(C)c2)(c2ccc(OCC(O)CO)c(C)c2)CC1
Reaction #337365
1-(4-(1-acetyl-4-[4-(2,3-dihydroxypropoxy)-3-methylphenyl]-piperidin-4-yl}-2-methylphenoxy)-3,3-dimethylbutan-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
Cc1cc([N+](=O)[O-])ccc1N=C1SC[C@H](CC(C)C)N1CC(=O)C(C)(C)C
Reaction #363625
(4S)-2-(2-methyl-4-nitrophenylimino)4-isobutyl-3-(2-oxo-3,3-dimethyl-1-butyl)-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CC(C)(C)OC(=O)N[C@@H]1CN(C2CCCCC2)c2ccccc2N(CC(=O)C(C)(C)C)C1=O
Reaction #439558
title compound
Yield 99.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
CC(C)(C)OC(=O)N1CC2CN(CC(=O)C(C)(C)C)CC(C1)O2
Reaction #498345
sub-title compound
Yield 85.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
CC(C)(C)C(=O)CN1CC2CN(CCCNc3ccc(C#N)cc3)CC(C1)O2
Reaction #498350
title compound
Yield 75.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
CC(C)(C)C(=O)CC1C(=O)N(N)c2ccccc2-c2ccccc21.Cl
Reaction #498540
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
CC(C)(C)C(=O)CC1C(=O)N(N)c2ccccc2-c2ccccc21.Cl
Reaction #501022
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
CC(C)(C)C(=O)CC1C(=O)N(N)c2ccccc2-c2ccccc21.Cl
Reaction #520583
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
CC(C)(C)C(=O)Cn1cncn1
Reaction #521560
3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-one
Yield 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_08
CN1CCN(c2nc(C(C)(C)C)cs2)CC1
Reaction #548959
2-(4-methyl-1-piperazinyl)-4-tert.butyl-thiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_12
CC(C)(C)C(=O)CC1C(=O)N(N)c2ccccc2-c2ccccc21.Cl
Reaction #567957
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
CC(C)(C)OC(=O)N1CC2CN(CC(=O)C(C)(C)C)CC(C1)O2
Reaction #587678
sub-title compound
Yield 85.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CC(C)(C)C(=O)CN1CC2CN(CCCNc3ccc(C#N)cc3)CC(C1)O2
Reaction #587683
title compound
Yield 75.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
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