2-cyanopyrazine

CC(C)(C)NC(=O)c1cnccn1
Reaction #3743
N-tert-butyl-2-pyrazine-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)NC(=O)c1cnccn1
Reaction #3744
N-tert-butyl-2-pyrazinecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1nccnc1Cl
Reaction #44982
title compound
Ausbeute 47.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
c1cnc(-c2ncc[nH]2)cn1
Reaction #155546
desired compound
Ausbeute 453.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
c1cnc(-c2n[nH]c(-c3cnccn3)n2)cn1
Reaction #214885
3,5-DIPYRAZINYL-1,2,4-TRIAZOLE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
c1cnc(-c2n[nH]c(-c3cnccn3)n2)cn1
Reaction #350305
3,5DIPYRAZINYL-1,2,4-TRIAZOLE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_05
N#Cc1nccnc1Cl
Reaction #369179
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
N#Cc1nccnc1Cl
Reaction #412785
title compound
Ausbeute 65.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_04
N#Cc1nccnc1Cl
Reaction #412786
title compound
Ausbeute 65.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_04
N#Cc1nccnc1Cl
Reaction #412788
title compound
Ausbeute 65.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_04
COC(=N)c1cnccn1
Reaction #414312
methyl pyrazinecarboximidate
Ausbeute 910.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
Cc1cc2c(Cl)nc(-c3cnccn3)nc2s1
Reaction #454961
4-chloro-2-(pyrazin-2-yl)-6-methyl-thieno-[2,3-d]-pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
Cc1csc2nc(-c3cnccn3)nc(Cl)c12
Reaction #454962
4-chloro-2-(pyrazin-2-yl)-5-methyl-thieno-[2,3-d]-pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CCc1cc2c(Cl)nc(-c3cnccn3)nc2s1
Reaction #454963
4-chloro-2-(pyrazin-2-yl)-6-ethyl-thieno-[2,3-d]-pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
Clc1cc2c(Cl)nc(-c3cnccn3)nc2s1
Reaction #454964
4-chloro-2-(pyrazin-2-yl)-6-chloro-thieno-[2,3-d]-pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
O=[N+]([O-])c1cc2c(Cl)nc(-c3cnccn3)nc2s1
Reaction #454965
4-chloro-2-(pyrazin-2-yl)-6-nitro-thieno-[2,3-d]-pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
Cc1sc2nc(-c3cnccn3)nc(Cl)c2c1C
Reaction #454966
4-chloro-2-(pyrazin-2-yl)-5,6-dimethyl-thieno-[2,3-d]-pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
FC(F)(F)c1cc2c(Cl)nc(-c3cnccn3)nc2s1
Reaction #454967
4-chloro-2-(pyrazin-2-yl)-6-trifluoromethyl-thieno-[2,3-d]-pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
COC(=N)c1cnccn1
Reaction #461367
methyl pyrazinecarboximidate
Ausbeute 910.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_11
O=c1nc(-c2cnccn2)sc2ccccc12
Reaction #586442
titled compound
Ausbeute 22.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
Seite 1Weiter