مشارك في 43 تفاعل

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O=C(Nc1ccc(OC(F)(F)F)cc1)c1cnc(N2CC[C@@H](O)C2)c(-c2cc[nH]n2)c1
Reaction #160911
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(Nc1ccc(OC(F)(F)F)cc1)c1cnc(N2CC[C@@H](O)C2)c(-c2ccnn2C2CCCCO2)c1
Reaction #160913
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(Nc1ccc(OC(F)(F)F)cc1)c1cnc(N2CC[C@@H](O)C2)c(Br)c1
Reaction #160914
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(=O)/C=C/c1cc(C(=O)Nc2ccc(OC(F)(F)F)cc2)cnc1N1CC[C@@H](O)C1
Reaction #160917
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cn1cc(-c2cc(C(=O)Nc3ccc(OC(F)(F)F)cc3)cnc2N2CC[C@@H](O)C2)cn1
Reaction #160923
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(Nc1ccc(OC(F)(F)F)cc1)c1cnc(N2CC[C@@H](O)C2)c(-c2ccc[nH]2)c1
Reaction #612828
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
O=C(Nc1ccc(OC(F)(F)F)cc1)c1cnc(N2CC[C@@H](O)C2)c(-c2ccoc2)c1
Reaction #612830
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
O=C(Nc1ccc(OC(F)(F)F)cc1)c1cnc(N2CC[C@@H](O)C2)c(-c2cnoc2)c1
Reaction #612831
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1ncc(-c2cc(C(=O)Nc3ccc(OC(F)(F)F)cc3)cnc2N2CC[C@@H](O)C2)s1
Reaction #612834
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
N#Cc1ccc(-c2cc(C(=O)Nc3ccc(OC(F)(F)F)cc3)cnc2N2CC[C@@H](O)C2)[nH]1
Reaction #612870
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
O=C(Nc1ccc(OC(F)(F)F)cc1)c1cnc(N2CC(O)C2)c(Br)c1
Reaction #612880
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1ncc(-c2cc(C(=O)Nc3ccc(OC(F)(F)F)cc3)cnc2N2CC[C@@H](O)C2)cn1
Reaction #1011036
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
O=C(Nc1ccc(OC(F)(F)F)cc1)c1cnc(N2CC[C@@H](O)C2)c(-c2cccnc2)c1
Reaction #1011039
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
Cc1ccc(-c2cc(C(=O)Nc3ccc(OC(F)(F)F)cc3)cnc2N2CC[C@@H](O)C2)cn1
Reaction #1011041
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
O=C(Nc1ccc(OC(F)(F)F)cc1)c1cnc(N2CC[C@@H](O)C2)c(-c2ccc(CO)nc2)c1
Reaction #1011042
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
Cc1ncccc1-c1cc(C(=O)Nc2ccc(OC(F)(F)F)cc2)cnc1N1CC[C@@H](O)C1
Reaction #1011043
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
Cc1cncc(-c2cc(C(=O)Nc3ccc(OC(F)(F)F)cc3)cnc2N2CC[C@@H](O)C2)c1
Reaction #1011044
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
O=C(Nc1ccc(OC(F)(F)F)cc1)c1cnc(N2CC[C@@H](O)C2)c(-c2cncc(F)c2)c1
Reaction #1011045
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
O=C(Nc1ccc(OC(F)(F)F)cc1)c1cnc(N2CC[C@@H](O)C2)c(-c2ccc(F)nc2)c1
Reaction #1011047
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
O=C(Nc1ccc(OC(F)(F)F)cc1)c1cnc(N2CC[C@@H](O)C2)c(-c2cnccc2F)c1
Reaction #1011048
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
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