2-methoxybenzyl chloride

CCOc1ccc2c(c1)c(-c1ccc3c(c1)OCO3)c(C(=O)OC)c(=O)n2Cc1ccccc1OC
Reaction #3003
methyl 4-(1,3-benzodioxol-5-yl)-1,2-dihydro-6-ethoxy-1-(2-methoxybenzyl)-2-oxoquinoline-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1COCCCCl
Reaction #177880
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccccc1COc1ccc(S(=O)(=O)c2ccc(C)nc2Br)cc1
Reaction #221146
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(Cl)c1ccccc1
Reaction #228162
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccccc1CN1CCN(CCO)CC1
Reaction #235153
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccccc1COCCCCCCN(C)C
Reaction #250230
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccccc1COCCCCCCN(C)C
Reaction #271270
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccccc1CN1CCN(C(=S)SC)CC1
Reaction #286007
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccccc1COc1cc(COC2CN(C(=O)OC(C)(C)C)CCC2c2ccc(OCCO)cc2)cc2ccccc12
Reaction #295503
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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Reaction #359978
hydrochloride salt
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COc1ccccc1COCCCCCCN(C)C
Reaction #359980
O-(2-methoxybenzyl)-6-dimethylaminohexanol
収率 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COc1ccccc1COCCCCCCN(C)C
Reaction #370835
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2cccc(Cl)c2)C(C(=O)NCCN(CC(N)=O)Cc2ccccc2OC)C1
Reaction #407112
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
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Reaction #488054
gum
収率 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
COc1ccccc1CNCc1ccccn1
Reaction #490290
N-(2-methoxybenzyl)-1-(pyridin-2-yl)methanamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
COc1ccccc1Cn1c2c(c3cc(C#N)ccc31)C[C@H](NC(=O)OC(C)C)C2
Reaction #537017
product
収率 98.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
COc1ccccc1CN1CCn2c(cc3cc(OC4CCN(C(C)C)CC4)ccc32)C1=O
Reaction #593881
desired product
収率 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
COc1ccccc1Cn1c2c(c3cc(C#N)ccc31)CC(NC(=O)C(C)C)CC2
Reaction #632698
off-white solid
収率 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
COc1ccccc1Cn1nc(-c2ccc(Cl)cc2)c2c1CCNCC2
Reaction #687124
title compound
収率 54.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
COc1ccc2ccc(S(=O)(=O)N(Cc3ccccc3OC)[C@H]3CCN(Cc4cccc(C#N)c4)C3=O)cc2c1
Reaction #706991
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_09
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