#929

O=C(Nc1cc(Nc2c(Cl)cnc3c2OCO3)ccn1)C1CC1
Reaction #135
Rendement 32.5%750 AstraZeneca ELN dataset
O=C(Nc1cc(Nc2c(Cl)cnc3c2OCO3)ccn1)C1CC1
Reaction #136
Rendement 32.2%750 AstraZeneca ELN dataset
O=C(Nc1cc(Nc2c(Cl)cnc3c2OCO3)ccn1)C1CC1
Reaction #137
Rendement 28.4%750 AstraZeneca ELN dataset
O=C(Nc1cc(Nc2c(Cl)cnc3c2OCO3)ccn1)C1CC1
Reaction #138
Rendement 70.9%750 AstraZeneca ELN dataset
O=C(Nc1cc(Nc2c(Cl)cnc3c2OCO3)ccn1)C1CC1
Reaction #139
Rendement 43.7%750 AstraZeneca ELN dataset
O=C(Nc1cc(Nc2c(Cl)cnc3c2OCO3)ccn1)C1CC1
Reaction #340
Rendement 59.1%750 AstraZeneca ELN dataset
COc1cc2c(Nc3c(Cl)cnc4c3OCO4)ncnc2cc1OCCCCl
Reaction #254533
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc2c(Nc3c(Cl)cnc4c3OCO4)ncnc2cc1OCC1CCN(C(=O)OC(C)(C)C)CC1
Reaction #2404794
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)
COc1cc2c(Nc3c(Cl)cnc4c3OCO4)ncnc2cc1OCCCCl
Reaction #2461603
title compound
Rendement 74.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12
COc1cc2c(Nc3c(Cl)cnc4c3OCO4)ncnc2cc1OCCCl
Reaction #2461604
title compound
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12
ClCCOc1cc(OC2CCOCC2)c2c(Nc3c(Cl)cnc4c3OCO4)ncnc2c1
Reaction #2461606
title compound
Rendement 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12
CC(C)Oc1cc(OCCCl)cc2ncnc(Nc3c(Cl)cnc4c3OCO4)c12
Reaction #2461607
title compound
Rendement 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12
COc1cc2ncnc(Nc3c(Cl)cnc4c3OCO4)c2cc1OCCCl
Reaction #2461608
title compound
Rendement 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12
COc1cc2ncnc(Nc3c(Cl)cnc4c3OCO4)c2cc1OCCCCl
Reaction #2461609
title compound
Rendement 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12
ClCCCOc1cc(OC2CCOCC2)c2c(Nc3c(Cl)cnc4c3OCO4)ncnc2c1
Reaction #2461610
title compound
Rendement 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12
COc1ccc(COc2cc(OC(C)C)c3c(Nc4c(Cl)cnc5c4OCO5)ncnc3c2)c(OC)c1
Reaction #2461611
title compound
Rendement 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12
ClCCCOc1ccc2c(Nc3c(Cl)cnc4c3OCO4)ncnc2c1
Reaction #2461612
title compound
Rendement 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12
O=C(O)c1ccnc2c1OCO2
Reaction #2461614
2,3-methylenedioxypyridine-4-carboxylic acid
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12
COc1cc2c(Nc3c(Cl)cnc4c3OCO4)ncnc2cc1OCC1CCN(C(=O)OC(C)(C)C)CC1
Reaction #2461621
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12