tert-butyl-5-amino-3-[2-(3,5-dimethoxyphenyl)ethyl]pyrazole-1-carboxylate

COc1cc(CCc2cc(NC(=O)c3ccccc3)[nH]n2)cc(OC)c1
Reaction #45005
title compound
Ausbeute 66.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(C(=O)Nc2cc(CCc3cc(OC)cc(OC)c3)n[nH]2)cc1
Reaction #45006
title compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3ccc(CN4CCC(F)CC4)cc3)[nH]n2)cc(OC)c1
Reaction #45007
title compound
Ausbeute 16.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3cccc(OC)c3)n[nH]2)cc(OC)c1
Reaction #45016
title compound
Ausbeute 59.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3ccc(CN(C)C)cc3)n[nH]2)cc(OC)c1
Reaction #45017
title compound
Ausbeute 28.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3ccc(OCCO)cc3)n[nH]2)cc(OC)c1
Reaction #45018
title compound
Ausbeute 12.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3ccc(CC(C)N)cc3)n[nH]2)cc(OC)c1
Reaction #45019
title compound
Ausbeute 4.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3ccc(CN4CCCC(F)C4)cc3)n[nH]2)cc(OC)c1
Reaction #45020
title compound
Ausbeute 16.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3ccc(N4CCNCC4)s3)n[nH]2)cc(OC)c1
Reaction #45021
title compound
Ausbeute 13.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3ccc(N4CC(C)NC(C)C4)cc3)[nH]n2)cc(OC)c1
Reaction #45041
title compound
Ausbeute 10.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3ccc(N4CCN(C)C(C)C4)cc3)n[nH]2)cc(OC)c1
Reaction #45043
title compound
Ausbeute 19.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3ccccc3NCc3cc(C)no3)n[nH]2)cc(OC)c1
Reaction #45046
title compound
Ausbeute 10.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3cnc(N4CCN(C)CC4)nc3)[nH]n2)cc(OC)c1
Reaction #45050
title compound
Ausbeute 0.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3ccc(C(=O)N4CCN(C)CC4)cc3)n[nH]2)cc(OC)c1
Reaction #45052
title compound
Ausbeute 56.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3ccc(N4CCN(C(C)C)CC4)cc3)n[nH]2)cc(OC)c1
Reaction #45054
title compound
Ausbeute 5.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3ccc(N4CCN(C5CC5)CC4)cc3)n[nH]2)cc(OC)c1
Reaction #45056
title compound
Ausbeute 12.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3ccc(N4CCN(C(C)=O)CC4)cc3)n[nH]2)cc(OC)c1
Reaction #45062
title compound
Ausbeute 1.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3ccc(C4CCN(C)CC4)cc3)n[nH]2)cc(OC)c1
Reaction #45067
title compound
Ausbeute 16.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3ccc(N4CCN5CCCC5C4)cc3)[nH]n2)cc(OC)c1
Reaction #45069
title compound
Ausbeute 10.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3ccc(N4CCN5CCCCC5C4)cc3)[nH]n2)cc(OC)c1
Reaction #45070
title compound
Ausbeute 9.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Seite 1Weiter