thiosemicarbazide

Cn1cc(-c2nnc(N)s2)c(Nc2ccc(Br)cc2F)c(F)c1=O
Reaction #44205
desired product
Rendement 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1c2ccccc2C(=O)C1Cc1n[nH]c(=S)[nH]c1=O
Reaction #46259
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
S=c1[nH]c(-c2ccc(I)cc2)cc2ccnn12
Reaction #47891
5-(4-Iodo-phenyl)-6H-pyrazolo[1,5-c]pyrimidine-7-thione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCc1nnc(N)s1
Reaction #55397
5-amino-2-methoxymethyl-(1,3,4)-thiadiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CC(=O)N(C)c1cccc(-c2ccc3nnc(N)n3n2)c1
Reaction #63907
desired compound
Rendement 25.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCN(C(C)=O)c1cccc(-c2ccc3nnc(N)n3n2)c1
Reaction #63909
desired compound
Rendement 14.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CC(=O)N(C)c1cccc(-c2ccc3nnc(N)n3n2)c1
Reaction #63927
yellow crystals
Rendement 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCC(=O)N(CC)c1cccc(-c2ccc3nnc(N)n3n2)c1
Reaction #63933
yellow crystals
Rendement 44.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
O=C(NC1CCCCC1)NC1CCCCC1
Reaction #93073
dicyclohexylurea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
c1ccc(CSc2nnn[nH]2)cc1
Reaction #95981
5-Benzylthio-1H-tetrazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
COCc1nnc(N)s1
Reaction #156739
5-(methoxymethyl)-1,3,4-thiadiazol-2-amine
Rendement 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)S(=O)(=O)c1ccc(-c2cnc(N)c(C(=O)NNC(N)=S)n2)cc1
Reaction #165832
resultant precipitate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
NNc1nc2c(s1)CCOc1cc(Br)ccc1-2
Reaction #171849
title compound
Rendement 70.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1CCS(=O)(=O)c2ccc(Br)cc21
Reaction #174860
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=S)NN=Cc1ncc([N+](=O)[O-])n1Cc1ccccc1
Reaction #178968
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=S)NNC(=O)c1ccc2cnc(F)cc2c1
Reaction #179852
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)CCC(=NNC(N)=S)c1ccccc1
Reaction #186943
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)c1cc(C=C2SC(=NNC(N)=S)NC2=O)cc(C(C)(C)C)c1O
Reaction #190638
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=S)NN=Cc1c[nH]nc1-c1ccc([N+](=O)[O-])o1
Reaction #196874
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=S)NN=c1c(=O)c2ccc(O)cc2c1=O
Reaction #196948
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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