N-benzylhexan-1-amine

CCCCCCN(Cc1ccccc1)C(=O)Cc1ccc(OCc2ccccc2C(=O)OC)cc1
Reaction #174350
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCN(Cc1ccccc1)C(=O)Cc1ccc(O)c(OC)c1
Reaction #176191
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCN(Cc1ccccc1)C(=O)CCc1ccc(O)cc1
Reaction #271906
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCN(Cc1ccccc1)C(=O)Cc1ccc(O)c(F)c1
Reaction #759195
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCCCCCN(Cc1ccccc1)C(=O)CCc1ccc(O)cc1
Reaction #987047
desired product
収率 71.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
CCCCCCN(Cc1ccccc1)C(=O)Cc1ccc(OCc2ccccc2C(=O)OC)cc1
Reaction #987054
Methyl 2-[(4-{2-[benzyl(hexyl)amino]-2-oxoethyl}phenoxy)methyl]benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
CCCCCCN(Cc1ccccc1)C(=O)COc1ccc(CC(OCC)C(=O)OCC)cc1
Reaction #1233726
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CCCCCCN(Cc1ccccc1)C(=O)Cc1cccc(OCc2ccccc2C(=O)OC)c1
Reaction #1636319
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
CCCCCCN(Cc1ccccc1)C(=O)COc1ccc(C[C@H](OCC)C(=O)OCC)cc1
Reaction #1812386
Ethyl(2S)-3-(4-{2-[benzyl(hexyl)amino]-2-oxoethoxy}phenyl)-2-ethoxypropanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_02
CCCCCCN(Cc1ccccc1)C(=O)COc1ccc(C[C@H](OCC)C(=O)OCC)cc1
Reaction #2196190
colourless oil
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_04
CCCCCCN(Cc1ccccc1)C(=O)Cc1cccc(OCc2ccccc2C(=O)OC)c1
Reaction #2199155
Methyl 2-[(3-{2-[benzyl(hexyl)amino]-2-oxoethyl}phenoxy)methyl]benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_04
CCCCCCN(Cc1ccccc1)C(=O)Cc1ccc(O)c(F)c1
Reaction #2199170
desired product
収率 77.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_04
CCCCCCN(Cc1ccccc1)C(=O)Cc1ccc(O)c(OC)c1
Reaction #2199173
desired product
収率 74.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_04
CCCCCCN(Cc1ccccc1)C(=O)CBr
Reaction #2199220
desired product
収率 58.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_04