Impliqué dans 25 réactions

187552

Cc1nc(Br)sc1C(=O)NCc1cccnc1
Reaction #180197
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1nc(N2CCC(Cc3ccc(F)cc3)C2=O)sc1C(=O)NCc1cccnc1
Reaction #262957
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1nc(Br)sc1C(=O)NCc1cccnc1
Reaction #270900
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1nc(Br)sc1C(=O)NCc1cccnc1
Reaction #291726
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1nc(Br)sc1C(=O)NCc1cccnc1
Reaction #647749
2-bromo-4-methyl-N-(pyridin-3-ylmethyl)thiazole-5-carboxamide
Rendement 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
Cc1nc(N2CCN(Cc3ccccc3)S2(=O)=O)sc1C(=O)NCc1cccnc1
Reaction #647979
title compound
Rendement 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
Cc1nc(Br)sc1C(=O)NCc1cccnc1
Reaction #763100
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Cc1nc(Br)sc1C(=O)NCc1cccnc1
Reaction #970319
title compound
Rendement 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
Cc1nc(N2CCC(Cc3ccc(F)cc3)C2=O)sc1C(=O)NCc1cccnc1
Reaction #970353
title compound
Rendement 33.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
Cc1nc(N2CCC(Cc3ccc(OC(F)(F)F)cc3)C2=O)sc1C(=O)NCc1cccnc1
Reaction #970354
title compound
Rendement 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
Cc1nc(-n2ccccc2=O)sc1C(=O)NCc1cccnc1
Reaction #1206606
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
Cc1nc(N2CCC(Cc3ccc(OC(F)(F)F)cc3)C2=O)sc1C(=O)NCc1cccnc1
Reaction #1235646
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
Cc1nc(-c2nnn(COCc3ccccc3)n2)sc1C(=O)NCc1cccnc1
Reaction #1299331
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
Cc1nc(Br)sc1C(=O)NCc1cccnc1
Reaction #1966363
2-bromo-4-methyl-thiazole-5-carboxylic acid (pyridine-3-ylmethyl)-amide
Rendement 96.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_11
Cc1nc(-c2ccn[nH]2)sc1C(=O)NCc1cccnc1
Reaction #1966364
4-methyl-2-(2H-pyrazol-3-yl)-thiazole-5-carboxylic acid (pyridine-3-ylmethyl)amide
Rendement 87.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_11
Cc1nc(Br)sc1C(=O)NCc1cccnc1
Reaction #1974428
2-bromo-4-methyl-N-(pyridin-3-ylmethyl)thiazole-5-carboxamide
Rendement 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
Cc1nc(-n2ccccc2=O)sc1C(=O)NCc1cccnc1
Reaction #1974479
title compound
Rendement 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
Cc1nc(-n2ccc(OCc3ccccc3)cc2=O)sc1C(=O)NCc1cccnc1
Reaction #1974486
title compound
Rendement 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
Cc1nc(Br)sc1C(=O)NCc1cccnc1
Reaction #2154522
2-bromo-4-methyl-N-(pyridin-3-ylmethyl)thiazole-5-carboxamide
Rendement 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_10
Cc1nc(N2CCN(Cc3ccccc3)S2(=O)=O)sc1C(=O)NCc1cccnc1
Reaction #2154754
title compound
Rendement 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_10
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