An 24 Reaktionen beteiligt

400867

CC(=O)CC(=O)CCc1ccc(NC(=O)CCCC(=O)NCCOCCOCCOCCC(=O)OC(C)(C)C)cc1
Reaction #203875
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)CCOCCOCCOCCN
Reaction #289292
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)CCOCCOCCOCCNC(=O)c1cccc(SCc2cccc(C(=O)Nc3ccc(N4CCCCC4)cc3-c3cc(C(=O)NCc4cccc(C(F)(F)F)c4)ccn3)c2)c1
Reaction #712456
tert-butyl 1-oxo-1-(3-(3-(4-(piperidin-1-yl)-2-(4-(3-(trifluoromethyl)-benzylcarbamoyl)pyridin-2-yl)phenylcarbamoyl)benzylthio)phenyl)-5,8,11-trioxa-2-azatetradecan-14-oate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
CC(C)(C)OC(=O)CCOCCOCCOCCNC(=O)c1cccc2[nH]ccc12
Reaction #712626
tert-butyl 1-(1H-indol-4-yl)-1-oxo-5,8,11-trioxa-2-azatetradecan-14-oate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
CN(CCN1CCC[C@H]1C(=O)NCCOCCOCCOCCC(=O)OC(C)(C)C)C(=O)c1cccc(C(=O)Nc2ccc(N3CCCCC3)cc2-c2cc(C(=O)N[C@H]3CCCc4ccccc43)ccn2)c1
Reaction #712639
tert-butyl 1-((S)-1-(2-(N-methyl-3-((4-(piperidin-1-yl)-2-(4-(((S)-1,2,3,4-tetrahydronaphthalen-1-yl)carbamoyl)pyridin-2-yl)phenyl)carbamoyl)benzamido)ethyl)pyrrolidin-2-yl)-1-oxo-5,8,11-trioxa-2-azatetradecan-14-oate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
CN(CCN1CCC[C@H]1C(=O)NCCOCCOCCOCCC(=O)O)C(=O)c1cccc(C(=O)Nc2ccc(N3CCCCC3)cc2-c2cc(C(=O)N[C@H]3CCCc4ccccc43)ccn2)c1
Reaction #712640
1-((S)-1-(2-(N-methyl-3-((4-(piperidin-1-yl)-2-(4-(((S)-1,2,3,4-tetrahydronaphthalen-1-yl)carbamoyl)pyridin-2-yl)phenyl)carbamoyl)benzamido)ethyl)pyrrolidin-2-yl)-1-oxo-5,8,11-trioxa-2-azatetradecan-14-oic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
CC(C)(C)OC(=O)CCOCCOCCOCCN
Reaction #1489844
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
CC(=O)CC(=O)CCc1ccc(NC(=O)CCCC(=O)NCCOCCOCCOCCC(=O)OC(C)(C)C)cc1
Reaction #1489845
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
CC(C)(C)OC(=O)CCOCCOCCOCCNC(=O)c1cccc(SCc2cccc(C(=O)Nc3ccc(N4CCCCC4)cc3-c3cc(C(=O)NCc4cccc(C(F)(F)F)c4)ccn3)c2)c1
Reaction #1495198
tert-butyl 1-oxo-1-(3-(3-(4-(piperidin-1-yl)-2-(4-(3-(trifluoromethyl)-benzylcarbamoyl)pyridin-2-yl)phenylcarbamoyl)benzylthio)phenyl)-5,8,11-trioxa-2-azatetradecan-14-oate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
CC(C)(C)OC(=O)CCOCCOCCOCCNC(=O)c1cccc2[nH]ccc12
Reaction #1495370
tert-butyl 1-(1H-indol-4-yl)-1-oxo-5,8,11-trioxa-2-azatetradecan-14-oate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
CN(CCN1CCC[C@H]1C(=O)NCCOCCOCCOCCC(=O)OC(C)(C)C)C(=O)c1cccc(C(=O)Nc2ccc(N3CCCCC3)cc2-c2cc(C(=O)N[C@H]3CCCc4ccccc43)ccn2)c1
Reaction #1495382
tert-butyl 1-((S)-1-(2-(N-methyl-3-((4-(piperidin-1-yl)-2-(4-(((S)-1,2,3,4-tetrahydronaphthalen-1-yl)carbamoyl)pyridin-2-yl)phenyl)carbamoyl)benzamido)ethyl)pyrrolidin-2-yl)-1-oxo-5,8,11-trioxa-2-azatetradecan-14-oate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
CN(CCN1CCC[C@H]1C(=O)NCCOCCOCCOCCC(=O)O)C(=O)c1cccc(C(=O)Nc2ccc(N3CCCCC3)cc2-c2cc(C(=O)N[C@H]3CCCc4ccccc43)ccn2)c1
Reaction #1495383
1-((S)-1-(2-(N-methyl-3-((4-(piperidin-1-yl)-2-(4-(((S)-1,2,3,4-tetrahydronaphthalen-1-yl)carbamoyl)pyridin-2-yl)phenyl)carbamoyl)benzamido)ethyl)pyrrolidin-2-yl)-1-oxo-5,8,11-trioxa-2-azatetradecan-14-oic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
CC(C)(C)OC(=O)CCOCCOCCOCCN
Reaction #2150429
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_10
CC(=O)CC(=O)CCc1ccc(NC(=O)CCCC(=O)NCCOCCOCCOCCC(=O)OC(C)(C)C)cc1
Reaction #2150430
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_10
CC(C)(C)OC(=O)CCOCCOCCOCCN
Reaction #2198702
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_04
CC(=O)CC(=O)CCc1ccc(NC(=O)CCCC(=O)NCCOCCOCCOCCC(=O)OC(C)(C)C)cc1
Reaction #2198703
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_04
CC(=O)N1c2ccc(C(=O)NCCOCCOCCOCCC(=O)OC(C)(C)C)cc2[C@H](Nc2ccc(Cl)cc2)C[C@@H]1C
Reaction #2254455
title compound
Ausbeute 102.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_06
CC(=O)N1c2ccc(C(=O)NCCOCCOCCOCCC(=O)OC(C)(C)C)cc2[C@H](Nc2ccc(N3CCOCC3)cc2)C[C@@H]1C
Reaction #2254456
title compound
Ausbeute 69.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_06
CCCCCCCCCCCCOC[C@H](CSC[C@H](NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)NCCOCCOCCOCCC(=O)OC(C)(C)C)OCCCCCCCCCCCC
Reaction #2292224
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_06
CCCCCCCCCCCCOC[C@H](CSC[C@H](N)C(=O)NCCOCCOCCOCCC(=O)O)NC(=O)CCCCCCCCCCC
Reaction #2292227
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_06
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