Substructure Search

977925

COc1cc(Nc2ncc3c(n2)O[C@H](c2ccccc2)CN(C)C3)ccc1-n1cnc(C)c1
Reaction #364
Yield 0.0%
COc1cc(Nc2ncc3c(n2)O[C@H](c2ccccc2)CN(C)C3)ccc1-n1cnc(C)c1
Reaction #365
Yield 15.0%
COc1cc(Nc2ncc3c(n2)O[C@H](c2ccccc2)CN(C)C3)ccc1-n1cnc(C)c1
Reaction #366
Yield 0.0%
COc1cc(Nc2ncc3c(n2)O[C@H](c2ccccc2)CN(C)C3)ccc1-n1cnc(C)c1
Reaction #367
Yield 30.4%
COc1cc(Nc2ncc3c(n2)O[C@H](c2ccccc2)CN(C)C3)ccc1-n1cnc(C)c1
Reaction #368
Yield 0.0%
COc1cc(Nc2ncc3c(n2)O[C@H](c2ccccc2)CN(C)C3)ccc1-n1cnc(C)c1
Reaction #369
Yield 6.8%
COc1cc(Nc2ncc3c(n2)O[C@H](c2ccccc2)CN(C)C3)ccc1-n1cnc(C)c1
Reaction #370
Yield 0.0%
COc1cc(Nc2ncc3c(n2)O[C@H](c2ccccc2)CN(CCF)C3)ccc1-n1cnc(C)c1
Reaction #371
Yield 14.9%
COc1nc(Cl)ncc1I
Reaction #66496
2-chloro-5-iodo-4-methoxy-pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccc(C(F)(F)F)c1)n1ccc2cc(Oc3ccnc(Cl)n3)ccc21
Reaction #73383
5-(2-chloropyrimidin-4-yloxy)-N-(3-(trifluoromethyl)phenyl)-1H-indole-1-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCc1nccc(Oc2ccc3[nH]ccc3c2)n1
Reaction #73451
(4-(1H-indol-5-yloxy)pyrimidin-2-yl)methyl acetate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Oc2nc(Nc3ccc(OCC(O)CN(C)C)cc3)ncc2Br)cc1
Reaction #78075
product
Yield 63.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Oc2nc(Cl)ncc2Br)cc1
Reaction #78078
product
Yield 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(Oc2nc(OC)cc(OC)n2)ccc2ocnc12
Reaction #80275
desired compound
Yield 39.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)COCc1cc(OCC2CC2)nc(Cl)n1
Reaction #87409
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Nc2nc(COCC(F)(F)F)cc(OCC3CC3)n2)ccc1-n1cnc(C)c1
Reaction #87457
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(N2CC3CCC(C2)O3)nc(Cl)n1
Reaction #162611
title compound
Yield 46.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccc(C(F)(F)F)c1)c1cccc2cc(Oc3ccnc(Cl)n3)ccc12
Reaction #173682
DOI: 10.1039/C8SC04228D
CCOc1nc(Cl)nc2c1oc1nc(-c3ccccc3)cc(C)c12
Reaction #176825
DOI: 10.1039/C8SC04228D
COc1nc(N)ncc1-c1nc(OC2CCOCC2)cc(N2CCOCC2)n1
Reaction #179425
DOI: 10.1039/C8SC04228D
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