An 194 Reaktionen beteiligt

NC1CCCc2ccccc21

c1ccc2c(c1)CCCC2Nc1nc2ccccc2[nH]1
Reaction #44828
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc2c(c1)CCN(CC(=O)NC1CCCc3ccccc31)C2Cc1ccc(OC)c(OC)c1
Reaction #76875
2-[1-(3,4-Dimethoxy-benzyl)-6-methoxy-3,4-dihydro-1H-isoquinolin-2-yl]-N-(1,2,3,4-tetrahydro-naphthalen-1-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1cc2c(cc1OC)C(Cc1ccccc1)N(CC(=O)NC1CCCc3ccccc31)CC2
Reaction #76879
2-(1-Benzyl-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl)-N-(1,2,3,4-tetrahydronaphthalen-1-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1cccc(CC2c3cc(OC)c(OC)cc3CCN2CC(=O)NC2CCCc3ccccc32)c1
Reaction #76888
2-[1-(3-Methoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-N-(1,2,3,4-tetrahydronaphthalen-1-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(CC2c3cc(OC)c(OC)cc3CCN2CC(=O)NC2CCCc3ccccc32)cc1
Reaction #76893
2-[1-(4-Methoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-N-(1,2,3,4-tetrahydronaphthalen-1-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(CC2c3cc(OC)c(OC)cc3CCN2CC(=O)NC2CCCc3ccccc32)cc1OC
Reaction #76900
2-[1-(3,4-Dimethoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-N-(1,2,3,4-tetrahydro-naphthalen-1-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(C[C@H]2c3cc(OC)c(OC)cc3CCN2CC(=O)NC2CCCc3ccccc32)cc1OC
Reaction #76923
2-[(1S)-1-(3,4-Dimethoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-N-(1,2,3,4-tetrahydronaphthalen-1-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(CC2c3cc(OC(C)C)c(OC)cc3CCN2CC(=O)NC2CCCc3ccccc32)cc1OC
Reaction #76963
2-[1-(3,4-Dimethoxy-benzyl)-6-methoxy-7-isopropoxy-3,4-dihydro-1H-isoquinolin-2-yl]-N-(1,2,3,4-tetrahydronaphthalen-1-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(CC2c3cc(OC(C)C)c(OC)cc3CCN2CC(=O)NC2CCCc3ccccc32)cc1OC
Reaction #76969
2-[1-(3,4-Dimethoxy-benzyl)-6-methoxy-7-isopropoxy-3,4-dihydro-1H-isoquinolin-2-yl]-N-(1,2,3,4-tetrahydronaphthalen-1-y)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1cc2c(cc1OC)C(Cc1ccc(N(C)C)cc1)N(CC(=O)NC1CCCc3ccccc31)CC2
Reaction #76993
2-[1-(4-Dimethylamino-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-N-(1,2,3,4-tetrahydro-naphthalen-1-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1cc2c(cc1OC)C(Cc1ccc(F)cc1)N(CC(=O)NC1CCCc3ccccc31)CC2
Reaction #76999
2-[1-(4-Fluoro-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-N-(1,2,3,4-tetrahydro-naphthalen-1-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(CC2c3c(cc(OC)c(OC)c3OC)CCN2CC(=O)NC2CCCc3ccccc32)cc1OC
Reaction #77005
2-[1-(3,4-Dimethoxy-benzyl)-6,7,8-trimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-N-(1,2,3,4-tetrahydro-naphthalen-1-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(CC2c3cc(OC)c(OC)c(OC)c3CCN2CC(=O)NC2CCCc3ccccc32)cc1OC
Reaction #77015
2-[1-(3,4-Dimethoxy-benzyl)-5,6,7-trimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-N-(1,2,3,4-tetrahydro-naphthalen-1-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1cc2c(c(OC)c1)C(Cc1ccc(OC)c(OC)c1)N(CC(=O)NC1CCCc3ccccc31)CC2
Reaction #77027
2-[1-(3,4-Dimethoxy-benzyl)-6,8-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-N-(1,2,3,4-tetrahydro-naphthalen-1-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1cc2c(cc1OC)C(Cc1ccc(OC)c(OC)c1OC)N(CC(=O)NC1CCCc3ccccc31)CC2
Reaction #77035
2-[1-(2,3,4-Trimethoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-N-(1,2,3,4-tetrahydro-naphthalen-1-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(CC2c3cc(OC)c(OC)cc3CCN2CC(=O)NC2CCCc3ccccc32)cc1Br
Reaction #77050
2-[1-(3-Bromo-4-methoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-N-(1,2,3,4-tetrahydro-naphthalen-1-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1nc(NCc2ccccn2)nc(NC2CCCc3ccccc32)c1C
Reaction #91405
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Nc1cc(-c2nc3ccccc3o2)ccc1NC1CCCc2ccccc21
Reaction #161449
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=[N+]([O-])c1ccc(Sc2cccc(CNC3CCCc4ccccc43)c2)cc1
Reaction #194401
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN1CCN(c2cc(-c3ccc4c(c3)CN(C(=O)NC3CCCc5ccccc53)CC4)nc(N)n2)CC1
Reaction #203983
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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