#8105052

Cc1ccncc1N1CCN(c2ccnc(C(F)(F)F)c2)C1=O
Reaction #167374
product
Выход 73.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Fc1ncccc1-c1ccnc(C(F)(F)F)c1
Reaction #560806
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
O=C1N(c2ccnc(C(F)(F)F)c2)CCN1c1cnccc1C1CC1
Reaction #610711
product
Выход 33.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
O=C(OCc1ccccc1)N1C(=O)N(c2ccnc(C(F)(F)F)c2)C2CC21
Reaction #610765
product
Выход 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
O=C1N(c2ccnc(C(F)(F)F)c2)CCN1c1cnccc1C1CC1
Reaction #659555
product
Выход 33.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
O=C(OCc1ccccc1)N1C(=O)N(c2ccnc(C(F)(F)F)c2)C2CC21
Reaction #659607
product
Выход 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CC(C)(C)OC(=O)NCc1ccn(-c2ccnc(C(F)(F)F)c2)c(=O)c1
Reaction #798446
tert-butyl (2-oxo-1-(2-(trifluoromethyl)pyridin-4-yl)-1,2-dihydropyridin-4-yl)methylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
Cn1cncc1C(O)c1ccnc(C(F)(F)F)c1
Reaction #1013671
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
Cn1cncc1C(O)c1ccnc(C(F)(F)F)c1
Reaction #1015990
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CCOC(=O)c1cn(-c2ccc(F)cc2)c2ccc(C#Cc3ccnc(C(F)(F)F)c3)cc2c1=O
Reaction #1136068
title compound
Выход 45.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
CC(C)(C)OC(=O)N1CCC2(CCN(c3ccnc(C(F)(F)F)c3)CC2)C1
Reaction #1200040
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CC(C)(C)OC(=O)N1CCC2(CCN(c3ccnc(C(F)(F)F)c3)CC2)C1
Reaction #1340880
desired product
Выход 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_06
NC1NC=C(Cl)C=C1c1ccc(Oc2ccnc(C(F)(F)F)c2)cc1
Reaction #1492911
title compound
Выход 55.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
COc1c(C(=O)NC2CCN(c3ccnc(C(F)(F)F)c3)CC2)n(C)c2c1c(=O)n(CC(=O)c1ccccc1)c1ccccc21
Reaction #1600792
title compound
Выход 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_07
NC1NC=C(Cl)C=C1c1ccc(Oc2ccnc(C(F)(F)F)c2)cc1
Reaction #1709844
title compound
Выход 55.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
NC1=NC(c2ccnc(C(F)(F)F)c2)(c2cc(Br)ccc2F)c2cccc(F)c21
Reaction #1749363
title compound
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_10
NC1=NC(c2ccnc(C(F)(F)F)c2)(c2ccc(F)c(Br)c2)c2cccc(F)c21
Reaction #1749365
title compound
Выход 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_10
COc1ccc(C2(c3ccnc(C(F)(F)F)c3)N=C(N)c3c(F)cccc32)cc1Br
Reaction #1749393
title compound
Выход 89.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_10
COc1cccc(C2(c3ccnc(C(F)(F)F)c3)N=C(N)c3c(F)cc(Cl)cc32)c1
Reaction #1749403
title compound
Выход 39.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_10
NC1NC=C(Cl)C=C1c1ccc(Oc2ccnc(C(F)(F)F)c2)cc1
Reaction #1835111
title compound
Выход 55.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_10
Страница 1Далее