1-(3-ethoxy-4-methoxyphenyl)-2-methylsulfonylethylamine

CCOc1cc(C(CS(C)(=O)=O)N2C(=O)c3cccc(NC(C)=O)c3C2=O)ccc1OC
Reaction #61056
product
Выход 59.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(=O)N[C@@H](CC(C)C)C(=O)O.CCOc1cc([C@H](N)CS(C)(=O)=O)ccc1OC
Reaction #61059
(S)-2-(3-ethoxy4-methoxyphenyl)-1-(methylsulphonyl)-eth-2-ylamine-N-acetyl-L-leucine salt
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOc1cc(C(CS(C)(=O)=O)N2C(=O)c3cccc(NC(C)=O)c3C2=O)ccc1OC
Reaction #84026
product
Выход 59.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(=O)N[C@@H](CC(C)C)C(=O)O.CCOc1cc([C@H](N)CS(C)(=O)=O)ccc1OC
Reaction #84029
(S)-2-(3-ethoxy-4-methoxyphenyl)-1-(methylsulphonyl)-eth-2-ylamine-N-acetyl-L-leucine salt
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOc1cc(C(CS(C)(=O)=O)N2C(=O)c3cccc(N(C)C)c3C2=O)ccc1OC
Reaction #198586
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOc1cc(C(CS(C)(=O)=O)N2C(=O)c3ccc(N(C)C)cc3C2=O)ccc1OC
Reaction #232098
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOc1cc(C(CS(C)(=O)=O)N2C(=O)c3cccc(OC)c3C2=O)ccc1OC
Reaction #408183
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOc1cc(C(CS(C)(=O)=O)N2Cc3ccccc3C2=O)ccc1OC
Reaction #463551
2-[1-(3-ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]isoindolin-1-one
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
CCOc1cc(C(CS(C)(=O)=O)N2C(=O)c3ccccc3C2=O)ccc1OC
Reaction #463553
2-[1-(3-ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]isoindoline-1,3dione
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
CCOc1cc(C(CS(C)(=O)=O)N2C(=O)c3ccc([N+](=O)[O-])cc3C2=O)ccc1OC
Reaction #463554
2-[1-(3-ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-5-nitro-isoindoline-1,3-dione
Выход 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
CCOc1cc(C(CS(C)(=O)=O)N2C(=O)c3cccc([N+](=O)[O-])c3C2=O)ccc1OC
Reaction #463556
2-[1-(3-ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-4-nitroisoindoline-1,3-dione
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
CCOc1cc(C(N)CS(C)(=O)=O)ccc1OC
Reaction #463557
1-(3-ethoxy-4-methoxyphenyl)-2-methylsulfonylethylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
CCOc1cc(C(CS(C)(=O)=O)N2C(=O)c3cccc(NC(C)=O)c3C2=O)ccc1OC
Reaction #463558
solid
Выход 59.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
—
Reaction #463559
solid
Выход 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
—
Reaction #463560
solid
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
—
Reaction #463561
solid
Выход 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
—
Reaction #463562
solid
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
—
Reaction #463563
solid
Выход 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
CCOc1cc(C(CS(C)(=O)=O)N2C(=O)c3cccc(NC(C)=O)c3C2=O)ccc1OC
Reaction #505728
product
Выход 59.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
CC(=O)N[C@@H](CC(C)C)C(=O)O.CCOc1cc([C@H](N)CS(C)(=O)=O)ccc1OC
Reaction #505731
(S)-2-(3-ethoxy-4-methoxyphenyl)-1-(methylsulphonyl)-eth-2-ylamine-N-acetyl-L-leucine salt
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
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