Participa en 162 reacciones

Cc1cnc(N)s1

Cc1cnc(Nc2nc(N[C@@H](C)c3ncc(F)cn3)nc(N3CCOCC3)n2)s1
Reaction #128
Rendimiento 20.7%750 AstraZeneca ELN dataset
Cc1cnc(Nc2cncc(Sc3ccc(NC(=O)C4CC4)cc3)n2)s1
Reaction #44475
title compound
Rendimiento 14.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cnc(NC(=O)c2cc(OCc3ccccc3)cc(O[C@@H](C)CO[Si](C)(C)C(C)(C)C)c2)s1
Reaction #48843
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Br.COCCn1cc(C)sc1=N
Reaction #165584
title compound
Rendimiento 40.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cn(CC2CCCO2)c(=N)s1
Reaction #165630
title compound
Rendimiento 86.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cn(CC2CCCCO2)c(=N)s1
Reaction #165635
title compound
Rendimiento 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COCCOCCn1cc(C)sc1=N
Reaction #165637
title compound
Rendimiento 83.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
[NH4+].[OH-]
Reaction #165647
NH4OH
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
[NH4+].[OH-]
Reaction #165656
NH4OH
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
[NH4+].[OH-]
Reaction #165657
NH4OH
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Br.C=CCn1cc(C)sc1=N
Reaction #165671
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
[NH4+].[OH-]
Reaction #165675
NH4OH
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cn(CCN2CCOCC2)c(=N)s1
Reaction #165720
title compound
Rendimiento 88.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)CC(=O)C[n+]1cc(C)sc1N.[Br-]
Reaction #169487
2-amino-3-(4-ethoxy-2,4-dioxobutyl)-5-methylthiazol-3-ium bromide
Rendimiento 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cnc(NC(=O)c2cccc3[nH]c(-c4cnccc4C(F)(F)F)nc23)s1
Reaction #172349
Compound 703
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cnc(NC(=O)C(=NOC2CCCC2)c2ccc(S(C)(=O)=O)c(Cl)c2)s1
Reaction #178202
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(Nc2cncnc2)c(C(=O)Nc2ncc(C)s2)n1
Reaction #183501
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cnc(NC(=O)c2cc(Br)ccc2O)s1
Reaction #213662
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cnc(NC(=O)C2=C(O)c3sc4ccccc4c3S(=O)(=O)N2C)s1
Reaction #215448
4-Hydroxy-2-methyl-N-(5-methyl-2-thiazolyl)-2H-[1]benzothieno[2,3-e]-1,2-thiazine-3-carboxamide-1,1-dioxide
Rendimiento 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
Cc1cnc(NC(=O)C2=C(O)c3sc4cc(Cl)ccc4c3S(=O)(=O)N2C)s1
Reaction #215475
7-Chloro-4-hydroxy-2-methyl-N-(5-methyl-2-thiazolyl)-2H-[1] benzothieno [2,3-e]-1,2-thiazine-3-carboxamide-1,1-dioxide
Rendimiento 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
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