Substructure Search

c1ccc(Cc2ccnnc2)cc1

O=c1ccn(-c2ccc3c(c2)Cc2cc(=O)[nH]nc2-3)cc1
Reaction #5898
title compound
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(Cc2ccnnc2)cc1
Reaction #178882
DOI: 10.1039/C8SC04228D
N#CC(c1ccccc1C(F)(F)F)c1cnn(C2CCCCO2)c(=O)c1Cl
Reaction #198268
DOI: 10.1039/C8SC04228D
O=c1cc(Cc2ccccc2C(F)(F)F)cn[nH]1
Reaction #228676
DOI: 10.1039/C8SC04228D
COC(=O)C(CC1CCCC1)n1ncc(Cc2ccccc2C(F)(F)F)cc1=O
Reaction #291123
DOI: 10.1039/C8SC04228D
O=C(O)c1cnncc1C(=O)c1cc(F)ccc1F
Reaction #321987
4-(2',5'-difluorobenzoyl)pyridazine-5-carboxylic acid
Yield 61.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(c2c(CO[Si](c3ccccc3)(c3ccccc3)C(C)(C)C)cc(C(=O)c3ccnnc3)c(F)c2Cl)C[C@H](C)O1
Reaction #332591
{5-({[tert-butyl(diphenyl)silyl]oxy}methyl)-3-chloro-4-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-2-fluorophenyl}(pyridazin-4-yl)methanone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cnncc1C(=O)c1cc(F)ccc1F
Reaction #392928
DOI: 10.1039/C8SC04228D
CCOc1nncc2c1C(c1ccc(C#N)cc1OC)C(C(C)=O)=C(C)N2
Reaction #398384
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1ccc(-c2cnn(CC(F)(F)F)c(=O)c2Cc2ccccc2)cc1
Reaction #407589
DOI: 10.1039/C8SC04228D
Cc1ccc(-n2nc(O)c3c(c2=O)Cc2ccc(Cl)cc2N3)cc1
Reaction #410830
title compound
Yield 97.1%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2c(c(O)nn1-c1ccc(O)cc1)Nc1cc(Cl)ccc1C2
Reaction #410831
title compound
Yield 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1nn(-c2ccc(C)cc2)c(=O)c2c1Nc1cc(Cl)ccc1C2
Reaction #410832
title compound
Yield 62.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-n2nc(O)c3c(c2=O)Cc2ccc(Cl)cc2N3)c(C)c1
Reaction #410833
title compound
Yield 39.4%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(Cc2ccnnc2)cc1
Reaction #426891
4-benzylpyridazine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1ccnnc1
Reaction #426892
phenylpyridazin-4-yl-methanone
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=S)NN=C(c2ccccc2)c2ccnnc2)CC1
Reaction #426893
yellow foamy solid 1A
Yield 99.3%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-c2cnn(-c3ccc(F)c(F)c3)c(=O)c2Cc2ccc(F)cc2)cc1
Reaction #469080
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-c2cnn(CC(F)(F)F)c(=O)c2Cc2ccc(F)cc2)cc1
Reaction #469082
title compound
Yield 28.0%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
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