5-chloro-pyrazine-2-carboxylic acid methyl ester

COc1cc(CCc2cc(NC(=O)c3cnc(N4CCN5CCCCC5C4)cn3)[nH]n2)cc(OC)c1
Reaction #45087
desired compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CC=C(c2cnc(C(=O)O)cn2)CC1
Reaction #45138
5-[1-[(2-methylpropan-2-yl)oxycarbonyl]-3,6-dihydro-2H -pyridin-4-yl]pyrazine-2-carboxylic acid
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1cnc(N2CCC(N(C(=O)c3ccc(-c4cnco4)cc3)C3CC3)CC2)cn1
Reaction #156058
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1cnc(Nc2ccc(Cl)c(Cl)c2)cn1
Reaction #164654
methyl 5-(3,4-dichlorophenylamino)pyrazine-2-carboxylate
Ausbeute 51.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1cnc(N2CCOCC2)cn1
Reaction #187029
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1cnc(OCc2ccc(C(C)C(O)(c3ccnc(Cl)c3)C(F)(F)F)c(Cl)c2)cn1
Reaction #191513
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)c1cnc(Cl)cn1
Reaction #218007
title compound
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
COC(=O)c1cnc(N2CC=C(c3nnc(Cc4ccccc4)c(C)c3C)CC2)cn1
Reaction #230953
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1cnc(Oc2ccc(C(C)C(O)(c3ccc4c(c3)N(C)C(=O)CO4)C(F)(F)F)c(Cl)c2)cn1
Reaction #245799
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(O)c1cnc(Cl)cn1
Reaction #266534
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1cnc(SC)cn1
Reaction #272245
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
NNC(=O)c1cnc(Cl)cn1
Reaction #276112
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1cnc(Oc2cc(C(=O)Nc3ccn(C)n3)cc3c2CC(C)(C)O3)cn1
Reaction #289948
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1cnc(Oc2ccc(Cl)c(C(C)C(O)(c3ccnc(Cl)c3)C(F)(F)F)c2)cn1
Reaction #290681
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COCCOC(=O)c1cnc(OCCOC)cn1
Reaction #305188
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CCOc1cnc(C(=O)O)cn1
Reaction #305196
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COC(=O)c1cnc(Oc2ccc3c(c2)CCN(C(=O)OC(C)(C)C)CC3)cn1
Reaction #309844
title compound
Ausbeute 58.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COC(=O)c1cnc(Oc2ccc3c(c2)CCN(C2CCC2)CC3)cn1
Reaction #309872
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
NC(=O)c1cnc(Cl)cn1
Reaction #315458
title compound
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COC(=O)c1cnc(N2CCN(c3nnc(-c4ccc(F)cc4)c(C)c3C)CC2C)cn1
Reaction #391369
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
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