Substructure Search

17175

c1cc2c(N3CCOCC3)nccc2cn1
Reaction #8834
1-morpholin-4-yl-[2,6]naphthyridine
DOI: 10.6084/m9.figshare.5104873.v1
Clc1cccc(Nc2nc3cnccc3c3cnccc23)c1
Reaction #197292
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccc(Nc2nccc3cnccc23)cc1)NC(=O)OC(C)(C)C
Reaction #207578
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccc(Oc2nccc3cnccc23)cc1)NC(=O)OC(C)(C)C
Reaction #208905
DOI: 10.1039/C8SC04228D
CC(C)c1nc2ccnc(Cl)c2c2cnccc12
Reaction #224623
DOI: 10.1039/C8SC04228D
Clc1nc2ccccc2c2cnccc12
Reaction #233588
DOI: 10.1039/C8SC04228D
Clc1nc2c(-c3nnc[nH]3)cccc2c2cnccc12
Reaction #237757
DOI: 10.1039/C8SC04228D
c1cc2c(N3CCOCC3)nccc2cn1
Reaction #265303
DOI: 10.1039/C8SC04228D
O=c1[nH]ccc2c(Nc3c(F)cc(F)cc3F)nc3ccc(Br)cc3c12
Reaction #291887
DOI: 10.1039/C8SC04228D
N#Cc1ccc2c(c1)nc(Cl)c1ccncc12
Reaction #398352
DOI: 10.1039/C8SC04228D
Cc1ccc(C(C)(C)C)cc1Nc1nc2ccc(F)cc2c2c(Cl)nccc12
Reaction #407035
DOI: 10.1039/C8SC04228D
O=C(Nc1cc2c(Cl)nc(-c3ccccc3Cl)cc2cn1)C1CC1
Reaction #556038
title compound
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1nc(-c2ccccc2Cl)cc2cnc(NC(=O)C3CC3)cc12
Reaction #556040
title compound
Yield 50.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(F)cc1-c1cc2cnc(NC(=O)C3CC3)cc2c(S(C)(=O)=O)n1
Reaction #556055
title compound
Yield 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1nc(-c2cc(F)ccc2C)cc2cnc(NC(=O)C3CC3)cc12
Reaction #556056
title compound
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(F)cncc1-c1cc2cnc(NC(=O)OC(C)(C)C)cc2c(C)n1
Reaction #556140
title compound
Yield 50.4%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #578733
solid
Yield 68.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #594886
solid
Yield 68.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(c1)nc(Cl)c1ccncc12
Reaction #620290
methyl 5-chlorobenzo[c][2,6]naphthyridine-8-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(c1)nc(Cl)c1ccncc12
Reaction #691534
methyl 5-chlorobenzo[c][2,6]naphthyridine-8-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
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