An 8 Reaktionen beteiligt

581721

COc1ccc(C2(OC(=O)NC(C)c3cccc4ccccc34)OC(=O)C(c3ccc4c(c3)OCO4)=C2Cc2cc(OC)c(OC)c(OC)c2)cc1
Reaction #235209
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(c1cccc2ccccc12)N1C(=O)OC(c2cc(C(C)(C)C)cc(C(C)(C)C)c2O)(C(F)(F)F)C1=O
Reaction #286071
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc2c(NC(=O)NC(C)c3cccc4ccccc34)ncnc2cc1OCC1CCN(C)CC1
Reaction #480423
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_10
COc1cc2nccc(Oc3ccc(NC(=O)NC(C)c4cccc5ccccc45)cc3)c2cc1OC
Reaction #1324810
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CC(NC(=O)NCC1CCN(Cc2ccc(Cl)c(Cl)c2)C1)c1cccc2ccccc12
Reaction #1363558
1-[1-(3,4-dichlorobenzyl)pyrrolidin-3-(RS)-ylmethyl]-3-[1-(naphth-1-yl)ethyl]urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_12
COc1cc2nccc(Oc3ccc(NC(=O)NC(C)c4cccc5ccccc45)cc3)c2cc1OC
Reaction #1944428
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_11
CC(NC(=O)NC1CN2CCC1CC2)c1cccc2ccccc12
Reaction #2362046
title compound
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_09
CC(NC(=O)NC1CN2CCC1CC2)c1cccc2ccccc12
Reaction #2368385
title compound
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_09