Участвует в 63 реакциях

7781

Cc1ccccc1COc1nccnc1N
Reaction #4389
2-amino-3-(2-methylbenzyloxy)pyrazine
Выход 41.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Cc1ccccc1CNc1nccnc1N
Reaction #4390
2-amino-3-(2-methylbenzylamino)pyrazine
Выход 19.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CS(C)=Nc1nccnc1Cl
Reaction #92887
2
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
Nc1ncc(Br)nc1Cl
Reaction #168677
5-Bromo-3-chloro-pyrazin-2-ylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1nccnc1-c1ccc(OC2CCCCC2)cc1
Reaction #174579
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CS(C)=Nc1nccnc1Cl
Reaction #295598
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Nc1nccnc1-c1ccc(OC2CCCCC2)nc1
Reaction #394653
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1cc(S(C)(=O)=O)ccc1-c1cn2ccncc2n1
Reaction #572834
2-(2-methoxy-4-methylsulfonylphenyl)imidazo[1,2-a]pyrazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_08
CCc1nc2c(Cl)nccn2c1C(=O)OC
Reaction #588166
title compound
Выход 25.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
COC(=O)c1cn2ccnc(Cl)c2n1
Reaction #600394
title compound
Выход 70.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
S=c1[nH]c2nccnc2s1
Reaction #634520
product
Выход 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
Nc1nccnc1-c1ccc(C(=O)NCc2ccccc2)cc1
Reaction #683117
desired product
Выход 59.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
Nc1nccnc1-c1ccc(C(=O)N[C@H](CO)c2cccc(Cl)c2)c(F)c1
Reaction #683118
desired product
Выход 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(C)(C)OC(=O)c1ccc(-c2nccnc2N)cc1F
Reaction #683135
tert-butyl 4-(3-aminopyrazin-2-yl)-2-fluorobenzoate
Выход 86.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
COC(=O)c1ccc(-c2nccnc2N)cc1F
Reaction #683170
methyl 4-(3-aminopyrazin-2-yl)-2-fluorobenzoate
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
COC(=O)c1ccc(-c2nccnc2N)cc1F
Reaction #683269
product
Выход 111.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
Cc1ccccc1COc1nccnc1N
Reaction #780595
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Nc1nccnc1NC1CC1
Reaction #794463
title compound
Выход 31.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
Nc1nccnc1NC1CC1
Reaction #794621
N2-cyclopropylpyrazine-2,3-diamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
Nc1nccnc1-c1ccc(Oc2ccccc2)cc1
Reaction #887063
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
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