(4-methoxyphenyl)methanamine

COc1ccc(CNc2ccnc(Nc3ccccc3)c2)cc1
Reaction #739
Ausbeute 67.7%750 AstraZeneca ELN dataset
COc1ccc(CNCCCOc2cccc(-c3noc4ccsc34)c2)cc1
Reaction #8743
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cl.NCCCOc1cccc2c(N)nccc12
Reaction #10598
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(CNc2nccc3c(NC4CCN(C(=O)OC(C)(C)C)CC4)cccc23)cc1
Reaction #10676
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CC(NCc1ccccc1)c1ccccc1
Reaction #42697
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(CNc2ccc3c(=O)c(Br)c(C(C)C)oc3c2[N+](=O)[O-])cc1
Reaction #42764
3-Bromo-2-isopropyl-7-(4-methoxybenzylamino)-8-nitro-chromen-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(CNC(=O)c2cnc(CNC(=O)OC(C)(C)C)c3c(OC)cc(OC)cc23)cc1
Reaction #42911
[6,8-dimethoxy-4-(4-methoxy-benzylcarbamoyl)-isoquinolin-1-ylmethyl]-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(CNC(=O)c2cnc(CNC(=O)OC(C)(C)C)c3cc(OC)c(OC)cc23)cc1
Reaction #42935
[6,7-Dimethoxy-4-(4-methoxy-benzylcarbamoyl)-isoquinolin-1-ylmethyl]-carbamic acid tert-butyl ester
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(CNC(=O)Cc2cnc(CNC(=O)OC(C)(C)C)c3cc(OC)c(OC)cc23)cc1
Reaction #42952
{6,7-dimethoxy-4-[(4-methoxy-benzylcarbamoyl)-methyl]-isoquinolin-1-ylmethyl}-carbamic acid tert-butyl ester
Ausbeute 80.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(CNc2c(-c3ccccc3)c(C)c(C#N)c3nc(C(=O)N(C)C)oc23)cc1
Reaction #45901
compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(CNc2nc(C)cc(C)c2C(N)=O)cc1
Reaction #49977
product
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
COc1ccc(Cn2cnc(-c3ccccc3)c2C(OC)OC)cc1
Reaction #60816
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1ccc(CNc2cc(Br)ncc2[N+](=O)[O-])cc1
Reaction #68930
title compound
Ausbeute 77.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(CN2Cc3cc(Cl)c(OC)cc3C2)cc1
Reaction #69680
5-chloro-6-methoxy-2-(4-methoxy-benzyl)-2,3-dihydro-1H-isoindole
Ausbeute 14.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(CN2C(=O)c3cccc(O)c3C2=O)cc1
Reaction #69686
title compound
Ausbeute 81.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(CNC(=O)c2ccccc2)cc1
Reaction #70066
N-(p-methoxybenzyl)benzamide
Ausbeute 80.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Nc1c(C(=O)OCc2ccccc2)c(=O)[nH]c2ccccc12
Reaction #72675
benzyl 4-amino-2-oxo-1,2-dihydroquinoline-3-carboxylate
Ausbeute 116.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
—
Reaction #72677
solid
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
N#Cc1c(N)c2ccccc2[nH]c1=O
Reaction #72680
4-amino-2-oxo-1,2-dihydroquinoline-3-carbonitrile
Ausbeute 25.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(CNc2c(C(=O)N(Cc3ccc(OC)cc3)Cc3ccc(OC)cc3)c(=O)[nH]c3ccccc23)cc1
Reaction #72684
N,N-bis(4-methoxybenzyl)-4-(4-methoxybenzylamino)-2-oxo-1,2-dihydroquinoline-3-carboxamide
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
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