N-acetyl-L-leucine

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
Ausbeute 90.0%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 #84029
(S)-2-(3-ethoxy-4-methoxyphenyl)-1-(methylsulphonyl)-eth-2-ylamine-N-acetyl-L-leucine salt
Ausbeute 90.0%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 #505731
(S)-2-(3-ethoxy-4-methoxyphenyl)-1-(methylsulphonyl)-eth-2-ylamine-N-acetyl-L-leucine salt
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
CC(C)(C)c1ccc2c(c1)CC[C@@H]2N
Reaction #538780
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CC(=O)N[C@@H](CC(C)C)C(=O)O.CCOc1cc([C@H](N)CS(C)(=O)=O)ccc1OC
Reaction #557081
(S)-2-(3-ethoxy-4-methoxyphenyl)-1-(methylsulphonyl)-eth-2-ylamine-N-acetyl-L-leucine salt
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CC(C)C[C@H](N)C(=O)O
Reaction #725709
L-leucine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_12
CC(C)(C)c1ccc2c(c1)CC[C@@H]2N
Reaction #743614
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
CC(=O)N[C@@H](CC(C)C)C(=O)O.CCOc1cc([C@H](N)CS(C)(=O)=O)ccc1OC
Reaction #987394
(S)-2-(3-ethoxy-4-methoxyphenyl)-1-(methylsulphonyl)-eth-2-ylamine-N-acetyl-L-leucine salt
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
CC(C)(C)c1ccc2c(c1)CC[C@@H]2N
Reaction #999820
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
CC(=O)N[C@@H](CC(C)C)C(=O)O.CCOc1cc([C@H](N)CS(C)(=O)=O)ccc1OC
Reaction #1006107
(S)-2-(3-ethoxy-4-methoxyphenyl)-1-(methylsulphonyl)-eth-2-ylamine-N-acetyl-L-leucine salt
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CC(=O)N[C@@H](CC(C)C)C(=O)O.CCOc1cc([C@H](N)CS(C)(=O)=O)ccc1OC
Reaction #1011815
(S)-2-(3-ethoxy-4-methoxyphenyl)-1-(methylsulphonyl)-eth-2-ylamine-N-acetyl-L-leucine salt
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CC(=O)N[C@@H](CC(C)C)C(=O)O.CCOc1cc([C@H](N)CS(C)(=O)=O)ccc1OC
Reaction #1137911
(S)-2-(3-ethoxy-4-methoxyphenyl)-1-(methylsulphonyl)-eth-2-ylamine-N-acetyl-L-leucine salt
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
CC(=O)N[C@@H](CC(C)C)C(=O)O.CCOc1cc([C@H](N)CS(C)(=O)=O)ccc1OC
Reaction #1149863
(S)-2-(3-ethoxy-4-methoxyphenyl)-1-(methylsulphonyl)-eth-2-ylamine-N-acetyl-L-leucine salt
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_11
CC(=O)N[C@@H](CC(C)C)C(=O)O.CCOc1cc([C@H](N)CS(C)(=O)=O)ccc1OC
Reaction #1265634
(S)-2-(3-ethoxy-4-methoxyphenyl)-1-(methylsulphonyl)-eth-2-ylamine-N-acetyl-L-leucine salt
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_10
CC(=O)N[C@@H](CC(C)C)C(=O)O.CCOc1cc([C@H](N)CS(C)(=O)=O)ccc1OC
Reaction #1341340
(S)-2-(3-ethoxy-4-methoxyphenyl)-1-(methylsulphonyl)-eth-2-ylamine-N-acetyl-L-leucine salt
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_06
CC(=O)N[C@@H](CC(C)C)C(=O)O.CCOc1cc([C@H](N)CS(C)(=O)=O)ccc1OC
Reaction #1359440
(S)-2-(3-ethoxy-4-methoxyphenyl)-1-(methylsulphonyl)-eth-2-ylamine-N-acetyl-L-leucine salt
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_04
CC(=O)N[C@@H](CC(C)C)C(=O)O.CCOc1cc([C@H](N)CS(C)(=O)=O)ccc1OC
Reaction #1454052
(S)-2-(3-ethoxy-4-methoxyphenyl)-1-(methylsulphonyl)-eth-2-ylamine-N-acetyl-L-leucine salt
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_02
CC(=O)N[C@@H](CC(C)C)C(=O)O.CCOc1cc([C@H](N)CS(C)(=O)=O)ccc1OC
Reaction #1530033
(S)-2-(3-ethoxy-4-methoxyphenyl)-1-(methylsulphonyl)-eth-2-ylamine-N-acetyl-L-leucine salt
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_02
CC(=O)N[C@@H](CC(C)C)C(=O)O.CCOc1cc([C@H](N)CS(C)(=O)=O)ccc1OC
Reaction #1530071
(S)-2-(3-ethoxy-4-methoxyphenyl)-1-(methylsulphonyl)-eth-2-ylamine-N-acetyl-L-leucine salt
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_02
COc1cc2c(cc1O)C(Cc1ccc(OC)c(OC)c1)NCC2
Reaction #1550155
(-)-7-hydroxy-6-methoxy-1-(3,4-dimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_07
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