Substructure Search

543016

O=c1ccc2cc(Oc3ccc(NCc4ccc(OC(F)(F)F)cc4)nn3)ccc2[nH]1
Reaction #164657
6-((6-((4-(trifluoromethoxy)benzyl)amino)pyridazin-3-yl)oxy)quinolin-2(1H)-one
Yield 8.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCOc2cc(Oc3ccc(C(=O)Nc4ccc(C(F)(F)F)cn4)cc3)c(C#N)cc21
Reaction #1713566
methyl 7-(4-((5-(trifluoromethyl)pyridin-2-yl)carbamoyl)phenoxy)-6-cyanochroman-4-carboxylate
Yield 11.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CO[Si](C)(C)C(C)(C)C)n1cc(C(=O)c2cc(N=C(c3ccccc3)c3ccccc3)ccn2)c2cnccc21
Reaction #1840228
title compound
Yield 64.1%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(C2CCN(c3cccnc3)CC2)cc1
Reaction #1950777
c1ccc(C2CCN(c3cccnc3)CC2)cc1
Reaction #1950778
c1ccc(C2CCN(c3cccnc3)CC2)cc1
Reaction #1950779
c1ccc(C2CCN(c3cccnc3)CC2)cc1
Reaction #1950780
c1ccc(C2CCN(c3cccnc3)CC2)cc1
Reaction #1950781
c1ccc(C2CCN(c3cccnc3)CC2)cc1
Reaction #1950782
c1ccc(C2CCN(c3cccnc3)CC2)cc1
Reaction #1950873
c1ccc(C2CCN(c3cccnc3)CC2)cc1
Reaction #1950874
c1ccc(C2CCN(c3cccnc3)CC2)cc1
Reaction #1950875
c1ccc(C2CCN(c3cccnc3)CC2)cc1
Reaction #1950876
c1ccc(C2CCN(c3cccnc3)CC2)cc1
Reaction #1950877
c1ccc(C2CCN(c3cccnc3)CC2)cc1
Reaction #1950878
c1ccc(C2CCN(c3cccnc3)CC2)cc1
Reaction #1950969
c1ccc(C2CCN(c3cccnc3)CC2)cc1
Reaction #1950970
c1ccc(C2CCN(c3cccnc3)CC2)cc1
Reaction #1950971
c1ccc(C2CCN(c3cccnc3)CC2)cc1
Reaction #1950972
c1ccc(C2CCN(c3cccnc3)CC2)cc1
Reaction #1950973
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