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1133172

CS(=O)(=O)c1ccc(-c2cnn(CC(F)(F)F)c(=O)c2-c2cc(Cl)cc(Cl)c2)cc1
Reaction #243079
DOI: 10.1039/C8SC04228D
COCCCNc1c(-c2ccc(S(C)(=O)=O)cc2)cnn(CC(F)(F)F)c1=O
Reaction #280318
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1ccc(-c2cnn(CC(F)(F)F)c(=O)c2N=[N+]=[N-])cc1
Reaction #284419
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1ccc(-c2cnn(CC(F)(F)F)c(=O)c2Cc2ccccc2)cc1
Reaction #407589
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1ccc(-c2cnn(CC(F)(F)F)c(=O)c2Cc2ccc(F)cc2)cc1
Reaction #469082
title compound
収率 28.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2c(-c3ccc(S(C)(=O)=O)cc3)cnn(CC(F)(F)F)c2=O)ccc1F
Reaction #469093
2-(2,2,2-trifluoroethyl)-4-(4-fluoro-3-methylphenyl)-5-[4-(methylsulfonyl)phenyl]-3(2H)-pyridazinone
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-c2cnn(CC(F)(F)F)c(=O)c2-c2cc(Cl)cc(Cl)c2)cc1
Reaction #469094
title compound
収率 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-c2cnn(CC(F)(F)F)c(=O)c2Cc2ccccc2)cc1
Reaction #469097
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)COc1c(-c2ccc(S(C)(=O)=O)cc2)cnn(CC(F)(F)F)c1=O
Reaction #469099
title compound
収率 79.9%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-c2cnn(CC(F)(F)F)c(=O)c2N=[N+]=[N-])cc1
Reaction #469101
2-(2,2,2-Trifluoroethyl)-4-azido-5-[4-(methylsulfonyl)phenyl]-3(2H)-pyridazinone
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-c2cnn(CC(F)(F)F)c(=O)c2Cc2ccc(F)cc2)cc1
Reaction #978501
title compound
収率 28.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2c(-c3ccc(S(C)(=O)=O)cc3)cnn(CC(F)(F)F)c2=O)ccc1F
Reaction #978512
2-(2,2,2-trifluoroethyl)-4-(4-fluoro-3-methylphenyl)-5-[4-(methylsulfonyl)phenyl]-3(2H)-pyridazinone
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-c2cnn(CC(F)(F)F)c(=O)c2-c2cc(Cl)cc(Cl)c2)cc1
Reaction #978513
title compound
収率 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-c2cnn(CC(F)(F)F)c(=O)c2Cc2ccccc2)cc1
Reaction #978516
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)COc1c(-c2ccc(S(C)(=O)=O)cc2)cnn(CC(F)(F)F)c1=O
Reaction #978518
title compound
収率 79.9%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-c2cnn(CC(F)(F)F)c(=O)c2N=[N+]=[N-])cc1
Reaction #978520
2-(2,2,2-Trifluoroethyl)-4-azido-5-[4-(methylsulfonyl)phenyl]-3(2H)-pyridazinone
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-c2cnn(CC(F)(F)F)c(=O)c2Cc2cccc(F)c2)cc1
Reaction #1217754
DOI: 10.1039/C8SC04228D
CC(C)(C)COc1c(-c2ccc(S(C)(=O)=O)cc2)cnn(CC(F)(F)F)c1=O
Reaction #1236425
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1ccc(-c2cnn(CC(F)(F)F)c(=O)c2Cc2ccc(F)cc2)cc1
Reaction #1328951
title compound
収率 28.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2c(-c3ccc(S(C)(=O)=O)cc3)cnn(CC(F)(F)F)c2=O)ccc1F
Reaction #1328962
2-(2,2,2-trifluoroethyl)-4-(4-fluoro-3-methylphenyl)-5-[4-(methylsulfonyl)phenyl]-3(2H)-pyridazinone
DOI: 10.6084/m9.figshare.5104873.v1
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