4-methylsulfanylaniline

COc1cc(-n2nc(-c3c(Cl)cccc3Cl)[nH]c2=O)ccc1C(=O)Nc1ccc(SC)cc1
Reaction #87576
desired product
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CSc1ccc(Nc2nc(Nc3ccc4cn[nH]c4c3)c3ccn(S(=O)(=O)c4ccc(C)cc4)c3n2)cc1
Reaction #174018
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1ccc(NC(=N)c2ccc(Cl)cc2)cc1
Reaction #174618
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1ccc(N=Cc2ccc(Cl)cc2)cc1
Reaction #180103
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1ccc(NS(=O)(=O)C(C)C)cc1
Reaction #192331
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1ccc(NC(=N)c2ccc(C(F)(F)F)cc2)cc1
Reaction #193540
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1ccc(Nc2cc(C(=O)O)ccn2)cc1
Reaction #203630
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C=Nc2ccc(SC)cc2)cc1
Reaction #227259
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CSc1ccc(Nc2cc(-c3ccccc3)nc(-c3ccccc3)n2)cc1
Reaction #236425
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CSc1ccc(NC(=N)c2ccc(F)cc2)cc1
Reaction #248038
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CSc1ccc(Nc2cc(-c3ccccc3)nc(N3CCC(O)CC3)n2)cc1
Reaction #256183
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CSc1ccc(NC(=N)c2ccccc2)cc1
Reaction #261099
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CSc1ccc(Nc2nc(C)nc3ccccc23)cc1
Reaction #263596
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CSc1ccc(Nc2nc(-c3ccccc3)cc(N3CCC(O)CC3)n2)cc1
Reaction #264654
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc2ncc(C#N)c(Nc3ccc(SC)cc3)c2cc1OC
Reaction #268343
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COCCN1C(=O)C(Nc2ccc(SC)cc2)=C(c2ccccc2)C1=O
Reaction #277456
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CSc1ccc(NC2CCN(C(C)CC#N)CC2)cc1
Reaction #299376
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CSc1ccc2c(c1)C(=O)C(=O)N2
Reaction #332316
5-(methylthio)-1H-indole-2,3-dione
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
—
Reaction #342146
compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CSc1ccc(Nc2ccccc2CC(=O)O)cc1
Reaction #364465
2-[(4-methylmercaptophenyl)amino]phenylacetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
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