An 100 Reaktionen beteiligt

362721

COC(=O)c1cscc1NC(=O)COc1ccc(-c2ncccn2)cc1
Reaction #42886
title compound
Ausbeute 59.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(-c2ncccn2)c(C(=O)N2CCC[C@H](C)[C@@H]2CNc2ccc(C(F)(F)F)cn2)c1
Reaction #89147
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(-c2ncccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CN2C(=O)c3ccccc3C2=O)c1
Reaction #89339
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(-c2ncccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CN2C(=O)c3ccccc3C2=O)n1
Reaction #89390
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C[C@@H]1CCCN(C(=O)c2cc(Cl)ccc2-c2ncccn2)[C@@H]1CN1C(=O)c2ccccc2C1=O
Reaction #89411
title compound
Ausbeute 67.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C[C@@H]1CCCN(C(=O)c2cc(F)ccc2-c2ncccn2)[C@@H]1CN1C(=O)c2ccccc2C1=O
Reaction #89448
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C[C@@H]1CCCN(C(=O)c2cc(F)ccc2-c2ncccn2)[C@@H]1CN1C(=O)c2ccccc2C1=O
Reaction #89454
title compound
Ausbeute 56.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C[C@@H]1CCCN(C(=O)c2cccc(F)c2-c2ncccn2)[C@@H]1CN1C(=O)c2ccccc2C1=O
Reaction #89459
title compound
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C[C@@H]1CCCN(C(=O)c2ccc(F)cc2-c2ncccn2)[C@@H]1CN1C(=O)c2ccccc2C1=O
Reaction #89466
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C[C@@H]1CCCN(C(=O)c2c(F)cccc2-c2ncccn2)[C@@H]1CN1C(=O)c2ccccc2C1=O
Reaction #89473
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C[C@@H]1CCCN(C(=O)c2cc(F)c(F)cc2-c2ncccn2)[C@@H]1CN1C(=O)c2ccccc2C1=O
Reaction #89481
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCC(CC)c1cc(C)nn2c(-c3sc(-c4ncccn4)cc3C)c(C)nc12
Reaction #173190
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CCC(Nc2ccc(-c3ncccn3)cc2)CC1
Reaction #186345
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CCC(c2ccc(-c3ncccn3)cc2)CC1
Reaction #205052
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CC2C3CCC4=CC(=O)CCC4=C3C(c3ccc(-c4ncccn4)cc3)CC2(C)C1C(=O)C1CC1
Reaction #211200
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC12Cn3cnc(-c4ccc(F)cc4)c3C=C1CCCC2C(O)c1ncccn1
Reaction #222137
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Clc1ccc(C2OC(COCc3ccccc3)C(OCc3ccccc3)C(OCc3ccccc3)C2OCc2ccccc2)cc1Cc1ccc(-c2ncccn2)s1
Reaction #287530
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Clc1ccc([C@@H]2O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)cc1Cc1ccc(-c2ncccn2)s1
Reaction #308182
1-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-4-chloro-3-(5-(2-pyrimidinyl)-2-thienylmethyl)benzene
Ausbeute 46.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Cc1ccc([C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1Cc1ccc(-c2ncccn2)s1
Reaction #308196
1-(β-D-glucopyranosyl)-4-methyl-3-(5-(2-pyrimidinyl)-2-thienylmethyl)benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COc1c(Cc2ccc(-c3ncccn3)s2)cc([C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)c2ccccc12
Reaction #308221
1-(β-D-glucopyranosyl)-3-(5-(2-pyrimidinyl)-2-thienylmethyl)-4-methoxynaphthalene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
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