3-mercapto-1,2,4-triazole

O=C(CSc1nc[nH]n1)c1ccc(OCc2c(F)cccc2F)cc1
Reaction #53294
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Br.Br.NCCCSc1nc[nH]n1
Reaction #55386
3-(3-aminopropylthio)-1,2,4-triazole dihydrobromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
O=C(CSc1nc[nH]n1)NC/C=C\COc1cc(CN2CCCCC2)ccn1
Reaction #80360
title compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(CCCSc1nc[nH]n1)NC/C=C\COc1cc(CN2CCCCC2)ccn1
Reaction #80361
title compound
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1ccc(-c2nc3ccc(C)cn3c2CSc2nc[nH]n2)cc1
Reaction #196742
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1cccc(OCCCSc2n[nH]c(C(F)(F)F)n2)c1
Reaction #199899
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1cccc(OCCCSc2n[nH]c(-c3ccccc3)n2)c1
Reaction #201264
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(CSc1nc[nH]n1)c1ccc(OCc2c(F)cccc2F)cc1
Reaction #208675
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1nc(SCC2CC2)n[nH]1
Reaction #223877
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
c1nc(SCC2CCCC2)n[nH]1
Reaction #241664
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
c1nc(SCC2CCCC2)n[nH]1
Reaction #242171
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCSc1nc[nH]n1
Reaction #243029
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
c1nc(SCC2CCCCC2)n[nH]1
Reaction #263532
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C#CCSc1nc[nH]n1
Reaction #266805
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
c1ccc2c(c1)OCCC2Sc1nc[nH]n1
Reaction #280915
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCN(CC)C(=O)Sc1ncn(C(=O)N(CC)CC)n1
Reaction #336036
pale yellow solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CC(=O)SCSc1ncn(C(c2ccccc2)(c2ccccc2)c2ccccc2)n1
Reaction #336759
3- acetylthiomethylthio-1-trityl-1,2,4-triazole
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
O=C(CSc1nc[nH]n1)c1ccc(OCc2c(F)cccc2F)cc1
Reaction #338729
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
c1nc(SCC2CC2)n[nH]1
Reaction #343463
3-cyclopropylmethylthio-1,2,4-triazole
Ausbeute 99.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_10
O=[N+]([O-])c1ccc(Sc2nc[nH]n2)cc1
Reaction #347531
3-(4-nitrophenylthio)-1,2,4-triazole
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
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