p-anisoyl chloride

COc1ccc(C(=O)NCCCSc2ccncc2)cc1
Reaction #6201
desired compound
Yield 78.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1ccc(C(=O)c2ccc(OC)cc2OC)cc1
Reaction #10212
(2,4-dimethoxy-phenyl)-(4-methoxy-phenyl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(C(=O)c2ccccc2F)cc1
Reaction #10213
(2-fluoro-phenyl)-(4-methoxy-phenyl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(C(=O)Nc2cc(OCc3cc(OC)cc(OC)c3)n[nH]2)cc1
Reaction #45032
title compound
Yield 20.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(C(=O)NC2(C(=O)NCCc3c(-c4ccccc4)c4cc(OC)ccc4c(=O)n3C)CC2)cc1
Reaction #46141
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #56965
solid
Yield 11.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1ccc(C(=O)N(C)OC)cc1
Reaction #58201
orange-coloured oil
Yield 93.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1ccc(C(=O)c2ccc(C)cc2C(=O)O)cc1
Reaction #58233
2-(4-methoxybenzoyl)-5-methylbenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1ccc(C(=O)N[C@@H](COCC2CCN(C(C)C)CC2)c2ccccc2)cc1.Cl
Reaction #60725
N-[(R)-2-(1-Isopropylpiperidine-4-ylmethoxy)-1-phenylethyl]-4-methoxybenzamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1ccc(C(=O)Nc2ccncc2)cc1
Reaction #62214
colorless solid
Yield 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1ccc(C(=O)N2CSCC2=O)cc1
Reaction #63187
3-(4-methoxybenzoyl)-4-oxothiazolidine
Yield 62.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
COc1ccc(C(=O)N2C(=O)CCC2(C)C(F)(F)F)cc1
Reaction #65735
N-(4-methoxyphenylcarbonyl)-5-(trifluoromethyl)-5-methylpyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COc1ccc(C(=O)Nc2ccc(Cl)nc2Cl)cc1
Reaction #68994
N-(2,6-dichloro-pyridin-3-yl)-4-methoxy-benzamide
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(C(=O)Nc2nc(C)c(C(=O)NCc3ccccc3)s2)cc1
Reaction #73635
title compound
Yield 10.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(C(=O)Nc2ccccc2NCC2CCN(c3ccncc3)CC2)cc1
Reaction #78116
title compound
Yield 17.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(C(=O)Nc2cccnc2NCC2CCN(c3ccncc3)CC2)cc1
Reaction #78119
title compound
Yield 15.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(C(=O)Nc2cnccc2NCC2CCN(c3ccncc3)CC2)cc1
Reaction #78126
title compound
Yield 6.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COC(=O)CNC(=O)c1ccc(OC)cc1
Reaction #87146
methyl 2-(4-methoxybenzamido)acetate
Yield 86.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1ccc2c(c1)C(C)(C)c1[nH]c3cc(C#N)ccc3c1C2=O
Reaction #89969
title compound
Yield 40.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1ccc(C(=O)NCc2ccc3c(c2)C(=O)N(C2CCC(=O)NC2=O)C3=O)cc1
Reaction #91741
N-[2-(2,6-dioxo-piperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-5-ylmethyl]-4-methoxy-benzamide
Yield 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
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