Substructure Search

CC(=O)Nc1cc(N)ncc1C

CC(=O)Nc1cc(Nc2cc(NC3CC3)n3ncc(C#N)c3n2)ncc1C
Reaction #821
Yield 10.6%
CCOC(=O)c1cnc(N(Cc2ccc(OC)cc2)c2ccc(N3CCOCC3)nc2)cc1NC(=O)C(F)(F)F
Reaction #911436
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cnc(N(Cc2ccc(OC)cc2)c2ccc(N3CCOCC3)nc2)cc1N
Reaction #1657973
DOI: 10.1039/C8SC04228D
CCN1C(=O)CCc2cnc(Nc3ccccc3)cc21
Reaction #1945147
1-ethyl-7-phenylamino-3,4-dihydro-1H-[1,6]naphthyridin-2-one
Yield 13.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N(Cc2ccc(OC)cc2)c2ccc(N3CCOCC3)nc2)cc1NC(=O)C(F)(F)F
Reaction #2122728
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N(Cc2ccc(OC)cc2)c2ccc(N3CCOCC3)nc2)cc1N
Reaction #2122729
title compound
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1