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1164580

Nc1cc(-c2cc(Cl)ccc2Oc2cc(F)c(S(=O)(=O)Nc3ncns3)cc2F)ccn1
Reaction #74516
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(-c2cc(Cl)ccc2Oc2cc(F)c(S(=O)(=O)Nc3ccncn3)cc2Cl)ccn1
Reaction #74535
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(-c2cc(Cl)ccc2Oc2cc(F)c(S(=O)(=O)Nc3nncs3)cc2Cl)ccn1
Reaction #74537
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1cc(-c2cc(Cl)ccc2Oc2ccc(S(=O)(=O)Nc3ncns3)cc2C#N)ccn1
Reaction #74540
product
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(-c2cc(Cl)ccc2Oc2cc(F)c(S(=O)(=O)Nc3cccnn3)cc2Cl)ccn1
Reaction #74546
product
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(-c2cc(Cl)ccc2O)ccn1
Reaction #74640
title compound
Ausbeute 109.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2cc(-c3cc(Cl)ccc3O)ccn2)CC1
Reaction #74652
product
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1cc(-c2cc(Cl)ccc2O)ccn1
Reaction #74663
4-chloro-2-[2-(dimethylamino)pyridin-4-yl]phenol
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(-c2cc(Cl)ccc2Oc2cc(F)c(S(=O)(=O)Nc3cccnn3)cc2Cl)ccn1
Reaction #241508
DOI: 10.1039/C8SC04228D
Nc1cc(-c2cc(Cl)ccc2O)ccn1
Reaction #403733
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCN(c2cc(-c3cc(Cl)ccc3O)ccn2)CC1
Reaction #751330
DOI: 10.1039/C8SC04228D
CN(C)c1cc(-c2cc(Cl)ccc2Oc2ccc(S(=O)(=O)Nc3ncns3)cc2C#N)ccn1
Reaction #905479
DOI: 10.1039/C8SC04228D
CC(=O)Nc1cc2c(cn1)COc1cc(OC[C@H](CC(C)C)NC(=O)OC(C)(C)C)c(Cl)cc1-2
Reaction #958140
(S)-tert-butyl (1-((2-acetamido-9-chloro-5H-chromeno[3,4-c]pyridin-8-yl)oxy)-4-methylpentan-2-yl)carbamate
Ausbeute 79.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(Cl)cc1-c1cc(N)nc(Nc2ccc(CO)cc2)c1
Reaction #1041215
DOI: 10.1039/C8SC04228D
COc1ccc(Cl)cc1-c1cc(N)nc(N)c1.O=C(O)C(F)(F)F
Reaction #1359276
4-(5-chloro-2-methoxy-phenyl)-pyridine-2,6-diamine trifluoroacetic acid salt
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1-c1cc(N)nc(Nc2ccc(Cl)cc2)c1
Reaction #1359277
title compound
Ausbeute 33.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(Cl)cc1-c1cc(N)nc(Nc2ccc(CO)cc2)c1
Reaction #1359278
title compound
Ausbeute 39.8%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(-c2cc(Cl)ccc2Oc2cc(F)c(S(=O)(=O)Nc3ncns3)cc2F)ccn1
Reaction #1489087
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(-c2cc(Cl)ccc2Oc2cc(F)c(S(=O)(=O)Nc3ccncn3)cc2Cl)ccn1
Reaction #1489106
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(-c2cc(Cl)ccc2Oc2cc(F)c(S(=O)(=O)Nc3nncs3)cc2Cl)ccn1
Reaction #1489108
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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