2-cyclopropylmethyl-6-(3-fluoro-4-methoxyphenyl)-4-(3-methanesulfonyloxypropyl)-2H-pyridazin-3-one

COc1ccc(-c2cc(CCCN3CCN(C)CC3)c(=O)n(CC3CC3)n2)cc1F
Reaction #8138
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(-c2cc(CCCN(C)C)c(=O)n(CC3CC3)n2)cc1F
Reaction #8139
title compound
Ausbeute 64.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(-c2cc(CCCN3CCN(C(=O)OC(C)(C)C)CC3)c(=O)n(CC3CC3)n2)cc1F
Reaction #8140
title compound
Ausbeute 76.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(-c2cc(CCCN(CCO)CCO)c(=O)n(CC3CC3)n2)cc1F
Reaction #8141
title compound
Ausbeute 13.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(-c2cc(CCCN)c(=O)n(CC3CC3)n2)cc1F
Reaction #8142
title compound
Ausbeute 67.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(-c2cc(CCCN3CCN(C)CC3)c(=O)n(CC3CC3)n2)cc1F
Reaction #1069995
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_03
COc1ccc(-c2cc(CCCN(C)C)c(=O)n(CC3CC3)n2)cc1F
Reaction #1069996
title compound
Ausbeute 64.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_03
COc1ccc(-c2cc(CCCN3CCN(C(=O)OC(C)(C)C)CC3)c(=O)n(CC3CC3)n2)cc1F
Reaction #1069997
title compound
Ausbeute 76.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_03
COc1ccc(-c2cc(CCCN(CCO)CCO)c(=O)n(CC3CC3)n2)cc1F
Reaction #1069998
title compound
Ausbeute 13.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_03
COc1ccc(-c2cc(CCCN3CCN(C)CC3)c(=O)n(CC3CC3)n2)cc1F
Reaction #1072214
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_03
COc1ccc(-c2cc(CCCN(C)C)c(=O)n(CC3CC3)n2)cc1F
Reaction #1072215
title compound
Ausbeute 64.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_03
COc1ccc(-c2cc(CCCN3CCN(C(=O)OC(C)(C)C)CC3)c(=O)n(CC3CC3)n2)cc1F
Reaction #1072216
title compound
Ausbeute 76.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_03
COc1ccc(-c2cc(CCCN(CCO)CCO)c(=O)n(CC3CC3)n2)cc1F
Reaction #1072217
title compound
Ausbeute 13.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_03
COc1ccc(-c2cc(CCCN(CCO)CCO)c(=O)n(CC3CC3)n2)cc1F
Reaction #1316111
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
COc1ccc(-c2cc(CCCN3CCN(C)CC3)c(=O)n(CC3CC3)n2)cc1F
Reaction #1435963
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_05
COc1ccc(-c2cc(CCCN(C)C)c(=O)n(CC3CC3)n2)cc1F
Reaction #1435964
title compound
Ausbeute 64.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_05
COc1ccc(-c2cc(CCCN3CCN(C(=O)OC(C)(C)C)CC3)c(=O)n(CC3CC3)n2)cc1F
Reaction #1435965
title compound
Ausbeute 76.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_05
COc1ccc(-c2cc(CCCN(CCO)CCO)c(=O)n(CC3CC3)n2)cc1F
Reaction #1435966
title compound
Ausbeute 13.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_05
COc1ccc(-c2cc(CCCN)c(=O)n(CC3CC3)n2)cc1F
Reaction #2407003
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)