2-chloro-3,5-dimethylpyrazine

Cc1cnc(-c2cccc3ccccc23)c(C)n1
Reaction #157940
2-(1-naphthyl)-3,5-dimethylpyrazine
Yield 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cnc(N2CC3CN(C(=O)c4ccccc4-c4ccccc4)CC3C2)c(C)n1
Reaction #331118
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cc1cnc(N2CCN(C(=O)OC(C)(C)C)CC2)c(C)n1
Reaction #382843
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1ccc(-c2ncc(C)nc2C)cc1
Reaction #619073
2-(4-methoxyphenyl)-3,5-dimethylpyrazine
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1cnc(-c2ccc3ccccc3c2)c(C)n1
Reaction #619074
2-(2-naphthyl)-3,5-dimethylpyrazine
Yield 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
C=Cc1ncc(C)nc1C
Reaction #678684
3,5-Dimethyl-2-vinylpyrazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
Cc1cnc(-c2ccc(N(c3ccccc3)c3ccccc3)cc2)c(C)n1
Reaction #1115537
pyrazine
Yield 30.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
Cc1cnc(-c2cccc3c2C[C@H](N(Cc2ccccc2)Cc2ccccc2)CO3)c(C)n1
Reaction #1186599
title compound
Yield 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
Cc1cnc(-c2ccc(Oc3ccccc3)cc2)c(C)n1
Reaction #1270938
3,5-Dimethyl-2-(4-phenoxyphenyl)pyrazine
Yield 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
Cc1cnc(N2CC3CN(C(=O)c4ccccc4-c4ccccc4)CC3C2)c(C)n1
Reaction #1612178
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07
Cc1cnc(-c2cccc3ccccc23)c(C)n1
Reaction #1861276
2-(1-naphthyl)-3,5-dimethylpyrazine
Yield 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_02
Cc1cnc(N2CCN(C(=O)OC(C)(C)C)CC2)c(C)n1
Reaction #1891186
3′,5′-dimethyl-2,3,5,6-tetrahydro[1,2′]bipyrazinyl-4-carboxylic acid tert-butyl ester
Yield 87.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
Cc1cnc(C)c(N=[N+]=[N-])n1
Reaction #1908971
solid
Yield 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_10
Cc1cnc(C)c(N=[N+]=[N-])n1
Reaction #1917956
solid
Yield 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_06
Cc1cnc(-c2cccc3ccccc23)c(C)n1
Reaction #2036016
2-(1-naphthyl)-3,5-dimethylpyrazine
Yield 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_03
Cc1cnc(-c2cccc3c2CC(N(Cc2ccccc2)Cc2ccccc2)CO3)c(C)n1
Reaction #2220021
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
Cc1cnc(-c2ccc(-c3cccc4ccccc34)cc2)c(C)n1
Reaction #2260921
3,5-Dimethyl-2-(4-naphthalen-1-yl-phenyl)pyrazine
Yield 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_06
Cc1cnc(-c2ccc(-c3ccc4ccccc4c3)cc2)c(C)n1
Reaction #2260923
3,5-Dimethyl-2-(4-naphthalen-2-yl-phenyl)pyrazine
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_06
Cc1cnc(-c2ccc3cc(-c4ccccc4)ccc3c2)c(C)n1
Reaction #2260926
3,5-Dimethyl-2-(6-phenylnaphthalen-2-yl)pyrazine
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_06
Cc1cnc(-c2ccc3ccc(-c4ccccc4)cc3c2)c(C)n1
Reaction #2260928
3,5-Dimethyl-2-(7-phenylnaphthalen-2-yl)pyrazine
Yield 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_06
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