2,4-dimethoxybenzylamine

COc1ccc(CN2C(=O)c3c(-c4ccccc4Cl)cc4[nH]c5ccc(OC)cc5c4c3C2=O)c(OC)c1
Reaction #11224
4-(2-Chlorophenyl)-2-(2,4-dimethoxybenzyl)-9-methoxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(CNc2ncccc2C#N)c(OC)c1
Reaction #48380
title compound
収率 72.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(CNc2cccnc2C#N)c(OC)c1
Reaction #48384
title compound
収率 73.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(CN2C(=O)c3cccc(O)c3C2=O)c(OC)c1
Reaction #69687
title compound
収率 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(CNC(=O)CN2CCc3cc(OC)c(OC)cc3C2Cc2ccc(OC)c(OC)c2)c(OC)c1
Reaction #76908
2-[1-(3,4-Dimethoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-N-(2,4-dimethoxy-benzyl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(CN2CC(C(=O)O)CC2=O)c(OC)c1
Reaction #87166
1-(2,4-dimethoxybenzyl)-5-oxopyrrolidine-3-carboxylic acid
収率 71.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1ccc(CNc2cnccc2C(=O)O)c(OC)c1
Reaction #91328
title compound
収率 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1ccc(CN[C@@H]2CO[C@H](C(c3ccccc3)c3ccccc3)C[C@H]2O)c(OC)c1
Reaction #166120
(2S,4R,5R)-2-benzhydryl-5-(2,4-dimethoxybenzylamino)-tetrahydropyran-4-ol
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC1C(=O)NCC1C(=O)O
Reaction #170664
titled compound
収率 174.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1ccc(CN2CC(C(=O)O)CC2=O)c(OC)c1
Reaction #170684
titled compound
収率 90.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
—
Reaction #170690
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=C(CNCc1ccc(OC)cc1OC)CO[Si](C)(C)C(C)(C)C
Reaction #170754
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)C1CN(Cc2ccc(OC)cc2OC)C(=O)C12CC2
Reaction #170765
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1ccc(CNc2nc(Cl)nc3c2ncn3C2CCCC2)c(OC)c1
Reaction #185473
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(CNC(=O)c2ccc(-c3ccccn3)s2)c(OC)c1
Reaction #186002
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(CNc2cnc3cc(OC)ccc3n2)c(OC)c1
Reaction #190564
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(CNc2cnc3ccc(C)cc3n2)c(OC)c1
Reaction #194348
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(CNc2ncnc3c2ncn3C2CC(CN=[N+]=[N-])C3OC(C)(C)OC32)c(OC)c1
Reaction #208186
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C=NCc1ccc(OC)cc1OC
Reaction #215066
imine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
CS(=O)(=O)Nn1c(=O)[nH]c2cc([N+](=O)[O-])c(N)cc2c1=O
Reaction #222660
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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