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1192737

COc1ccc(-c2nn(CC3CCCC3)c(=O)c(C#N)c2-c2ccc(OC)cc2)cc1
Reaction #190801
DOI: 10.1039/C8SC04228D
COc1ccc(-c2nn(Cc3ccccc3)c(=O)c(C#N)c2-c2ccc(OC)cc2)cc1
Reaction #190931
DOI: 10.1039/C8SC04228D
COc1ccc(-c2nn(CC(C)C)c(=O)c(C#N)c2-c2ccc(OC)cc2)cc1
Reaction #193693
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)CCn1nc(-c2ccccc2)c(-c2ccccc2)c(C#N)c1=O
Reaction #197535
DOI: 10.1039/C8SC04228D
COc1ccc(-c2nn(C(C)C)c(=O)c(C#N)c2-c2ccc(OC)cc2)cc1
Reaction #255531
DOI: 10.1039/C8SC04228D
N#Cc1c(-c2ccccc2)c(-c2ccccc2)n[nH]c1=O
Reaction #551145
4-Cyano-5,6-diphenyl-3-(2H)-pyridazinone
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1c(-c2ccccc2)c(-c2ccccc2)n[nH]c1=O
Reaction #551146
4-Carboxy-5,6-diphenyl-3-(2H)-pyridazinone
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(-c2ccccc2)c(-c2ccccc2)nn(CCO)c1=O
Reaction #551149
solid
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)n1nc(-c2ccccc2)c(-c2ccccc2)c(C#N)c1=O
Reaction #551150
solid
DOI: 10.6084/m9.figshare.5104873.v1
N#CCCn1nc(-c2ccccc2)c(-c2ccccc2)c(C#N)c1=O
Reaction #551151
2-(2'-Cyanoethyl)-4-cyano-5,6-diphenyl-3-(2H)-pyridazinone
DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)CCn1nc(-c2ccccc2)c(-c2ccccc2)c(C#N)c1=O
Reaction #551152
solid
Ausbeute 72.7%DOI: 10.6084/m9.figshare.5104873.v1
CCC(Cn1nc(-c2ccccc2)c(-c2ccccc2)c(C#N)c1=O)[N+](=O)[O-]
Reaction #551153
white-yellow solid
Ausbeute 38.2%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(-c2ccccc2)c(-c2ccccc2)nn(CCS(=O)(=O)O)c1=O.O
Reaction #551154
yellow solid
Ausbeute 50.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2nn(CC3CC3)c(=O)c(C#N)c2-c2ccc(OC)cc2)cc1
Reaction #888503
DOI: 10.1039/C8SC04228D
CCC(Cn1nc(-c2ccccc2)c(-c2ccccc2)c(C#N)c1=O)[N+](=O)[O-]
Reaction #898031
DOI: 10.1039/C8SC04228D
COc1ccc(-c2nn(CC3CCCCC3)c(=O)c(C#N)c2-c2ccc(OC)cc2)cc1
Reaction #1028191
DOI: 10.1039/C8SC04228D
O=C(O)c1c(-c2ccccc2)c(-c2ccccc2)n[nH]c1=O
Reaction #1303276
DOI: 10.1039/C8SC04228D
N#CCCn1nc(-c2ccccc2)c(-c2ccccc2)c(C#N)c1=O
Reaction #1632472
DOI: 10.1039/C8SC04228D
COc1ccc(-c2nn(CC3CC3)c(=O)c(C#N)c2-c2ccc(OC)cc2)cc1
Reaction #1927444
title compound
Ausbeute 71.5%DOI: 10.6084/m9.figshare.5104873.v1
CCn1nc(-c2ccc(OC)cc2)c(-c2ccc(OC)cc2)c(C#N)c1=O
Reaction #1927445
title compound
Ausbeute 76.8%DOI: 10.6084/m9.figshare.5104873.v1
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