#1041432

NS(=O)(=O)c1cccc(Nc2cnccn2)c1
Reaction #546
收率 42.3%750 AstraZeneca ELN dataset
CC(Nc1cnccn1)c1ccccc1
Reaction #563
收率 42.5%750 AstraZeneca ELN dataset
CC(C)(C)OC(=O)N1CCCCC1CNc1cnccn1
Reaction #46359
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
NCCCNc1cnccn1
Reaction #55135
2-(3-aminopropylamino)-pyrazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CN(N)c1cnccn1
Reaction #67579
N-Methyl-N-pyrazin-2-yl-hydrazine
收率 35.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(=O)Nc1nc2c(s1)CN(c1cnccn1)CC2
Reaction #67640
N-(5-(pyrazin-2-yl)-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridin-2-yl)acetamide
收率 9.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CNCC(c1ccc(Br)cc1)c1ccc(Oc2cnccn2)cc1
Reaction #73800
desired product
收率 68.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=[N+]([O-])c1cnc(Sc2cnccn2)s1
Reaction #74896
((5-nitro-2-thiazolyl)thio)Pyrazine
收率 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
COc1ccc(CC2c3cc(Oc4cnccn4)c(OC)cc3CCN2CC(=O)NC2CCc3ccccc32)cc1OC
Reaction #77141
2-[1-(3,4-dimethoxy-benzyl)-6-methoxy-7-(pyrazin-2-yloxy)-3,4-dihydro-1H-isoquinolin-2-yl]-N-(indan-1-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=Cc1cn(-c2cnccn2)cn1
Reaction #78855
title compound
收率 99.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
FC(F)(F)c1ccc(Nc2cnccn2)cn1
Reaction #163263
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)N1CCN(c2cnccn2)CC1
Reaction #168093
4-Isopropyl-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
OC(c1cccnc1)c1nccnc1Cl
Reaction #168654
(3-chloro-pyrazin-2-yl)-pyridin-3-yl-methanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CN(C)CCC(Oc1cnccn1)c1ccccc1
Reaction #176086
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CC1OB(O)c2cc(Oc3cnccn3)cc(C)c21
Reaction #182138
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc(-c2cnccn2)cc1
Reaction #183634
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(NC(=O)OC(C)(C)C)CCN(c2cnccn2)CC1
Reaction #185497
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OC1(c2nccnc2Cl)CN2CCC1CC2
Reaction #187838
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(NC(=O)OC(C)(C)C)c1cccc(Oc2cnccn2)c1
Reaction #189053
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OC(c1ccc2ccc(-c3ccccc3)nc2c1)c1nccnc1Cl
Reaction #196763
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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