2-methylpropane-2-sulfinamide

CC(C)(C)/C=C/C=N/S(=O)C(C)(C)C
Reaction #40878
title compound
Rendimiento 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #40879
solid
Rendimiento 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)S(=O)/N=C/c1cc(C(F)(F)F)ccc1C(F)(F)F
Reaction #40880
N-{(1E)-[2,5-bis(trifluoromethyl)phenyl]methylene}-2-methylpropane-2-sulfinamide
Rendimiento 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)S(=O)NC1(Cc2ccccc2)CCC(Oc2ccc3c(c2)CCC(c2ccccc2)O3)CC1
Reaction #88059
2-methyl-propane-2-sulfinic acid [1-benzyl-4-(2-phenyl-chroman-6-yloxy)-cyclohexyl]-amide
Rendimiento 43.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1cccc(C(=NS(=O)C(C)(C)C)c2cc(Cl)cc(F)c2C#N)c1
Reaction #173304
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)c1cnc(C=NS(=O)C(C)(C)C)s1
Reaction #179234
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)S(=O)N=C(C1CC1)C1CC1
Reaction #181558
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=NS(=O)C(C)(C)C)c1ccc(Br)c(C)c1
Reaction #184355
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(S(=O)(=O)n2ccc3nc(C=NS(=O)C(C)(C)C)cnc32)cc1
Reaction #184836
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)S(=O)N=CC1CC1
Reaction #188744
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(NS(=O)C(C)(C)C)c1ccc(N)c([N+](=O)[O-])c1
Reaction #192115
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)S(=O)N=C(c1cccc(Br)c1)c1cccnc1C#N
Reaction #194449
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1cc(C(C)NS(=O)C(C)(C)C)ccc1NS(C)(=O)=O
Reaction #201601
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)S(=O)N=C1CC2(CCCOC2)Oc2ccc(Br)cc21
Reaction #212500
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)S(=O)N=C1CCC2(CC1)OCCO2
Reaction #219277
Compound 15
Rendimiento 45.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCC(C)CC(C)=NS(=O)C(C)(C)C
Reaction #221091
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)S(=O)N=CC1(C(F)(F)F)CCC(O[Si](C)(C)C(C)(C)C)CC1
Reaction #221707
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(CO[Si](C)(C)C(C)(C)C)=NS(=O)C(C)(C)C
Reaction #225416
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)S(=O)N=Cc1cc(C(F)(F)F)ccc1C(F)(F)F
Reaction #226504
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(c1ccc(Br)cc1)N(CCCC(=NS(=O)C(C)(C)C)c1ccccc1)C(=O)OC(C)(C)C
Reaction #226850
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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