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1387889

CC(=O)c1cnc(-c2ccccc2)c(-c2ccccc2)n1
Reaction #40845
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)c1cnc(-c2ccccc2)c(-c2ccccc2)n1
Reaction #40846
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NN1CCCCC1)c1cnc(-c2ccccc2)c(-c2ccccc2)n1
Reaction #211020
DOI: 10.1039/C8SC04228D
CC(=O)c1cnc(-c2ccccc2)c(-c2ccccc2)n1
Reaction #242288
DOI: 10.1039/C8SC04228D
CN(C)c1ccc(-c2nc(C(=O)O)c(N)nc2-c2ccc(S(C)(=O)=O)cc2)cc1
Reaction #556323
3-amino-6-[4-(dimethylamino)phenyl]-5-[4-(methylsulfonyl)phenyl]pyrazine-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cnc(-c2ccccc2)c(-c2ccccc2)n1
Reaction #1479304
crude product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cnc(-c2ccc(Br)cc2)c(-c2ccc(Br)cc2)n1
Reaction #1479305
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NN1CCCCC1)c1cnc(-c2ccccc2)c(-c2ccccc2)n1
Reaction #1479307
subtitle compound
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NN1CCCCC1)c1cnc(-c2ccc(Br)cc2)c(-c2ccc(Br)cc2)n1
Reaction #1479308
subtitle compound
Ausbeute 5.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cnc(-c2ccccc2)c(-c2ccccc2)n1
Reaction #1539688
crude product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cnc(-c2ccc(Br)cc2)c(-c2ccc(Br)cc2)n1
Reaction #1539689
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NN1CCCCC1)c1cnc(-c2ccccc2)c(-c2ccccc2)n1
Reaction #1539691
subtitle compound
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NN1CCCCC1)c1cnc(-c2ccc(Br)cc2)c(-c2ccc(Br)cc2)n1
Reaction #1539692
subtitle compound
Ausbeute 5.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cnc(-c2ccc(C)cc2)c(-c2ccc(C)cc2)n1
Reaction #2139973
yellow solid
DOI: 10.6084/m9.figshare.5104873.v1