N-[4-(trifluoromethyl)phenyl]-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-4-amine

Cc1ccccc1N1CCc2c(ncnc2Nc2ccc(C(F)(F)F)cc2)C1
Reaction #174121
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Fc1cccnc1N1CCc2c(ncnc2Nc2ccc(C(F)(F)F)cc2)C1
Reaction #197970
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cccc(N2CCc3c(ncnc3Nc3ccc(C(F)(F)F)cc3)C2)c1
Reaction #202582
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
FC(F)(F)c1ccc(Nc2ncnc3c2CCN(c2ccccc2)C3)cc1
Reaction #255889
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(N2CCc3c(ncnc3Nc3ccc(C(F)(F)F)cc3)C2)cc1
Reaction #386140
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CS(=O)(=O)c1cccnc1N1CCc2c(ncnc2Nc2ccc(C(F)(F)F)cc2)C1
Reaction #400396
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
FC(F)(F)c1ccc(Nc2ncnc3c2CCN(c2ccccc2)C3)cc1
Reaction #780901
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
FC(F)(F)c1ccc(Nc2ncnc3c2CCN(c2ncccc2Cl)C3)cc1
Reaction #1036464
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
FC(F)(F)c1ccc(Nc2ncnc3c2CCN(c2ncccc2Cl)C3)cc1
Reaction #1058371
white solid
المردود 57.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_12
CS(=O)(=O)c1cccnc1N1CCc2c(ncnc2Nc2ccc(C(F)(F)F)cc2)C1
Reaction #1058382
desired compound
المردود 49.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_12
Fc1cccnc1N1CCc2c(ncnc2Nc2ccc(C(F)(F)F)cc2)C1
Reaction #1058383
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_12
FC(F)(F)c1ccc(Nc2ncnc3c2CCN(c2ncccc2C(F)(F)F)C3)cc1
Reaction #1058384
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_12
CC(C)S(=O)(=O)c1cccnc1N1CCc2c(ncnc2Nc2ccc(C(F)(F)F)cc2)C1
Reaction #1058397
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_12
FC(F)(F)c1ccc(Nc2ncnc3c2CCN(c2ccccc2)C3)cc1
Reaction #1058424
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_12
Cc1ccccc1N1CCc2c(ncnc2Nc2ccc(C(F)(F)F)cc2)C1
Reaction #1058425
desired product
المردود 8.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_12
Cc1cccc(N2CCc3c(ncnc3Nc3ccc(C(F)(F)F)cc3)C2)c1
Reaction #1058426
desired product
المردود 17.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_12
Cc1ccc(N2CCc3c(ncnc3Nc3ccc(C(F)(F)F)cc3)C2)cc1
Reaction #1058427
desired product
المردود 17.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_12
Cc1cccc(N2CCc3c(ncnc3Nc3ccc(C(F)(F)F)cc3)C2)c1
Reaction #1200145
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CC(C)S(=O)(=O)c1cccnc1N1CCc2c(ncnc2Nc2ccc(C(F)(F)F)cc2)C1
Reaction #1228214
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
FC(F)(F)c1ccc(Nc2ncnc3c2CCN(c2ncccc2C(F)(F)F)C3)cc1
Reaction #2215289
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
الصفحة 1التالي