product

CCc1ccc(CCOc2ccc(C[C@H]3SC(=O)NC3=O)cc2)nc1.Cl
Reaction #969885
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CCc1ccc(CCOc2ccc(C[C@H]3SC(=O)NC3=O)cc2)nc1.O=C(O)[C@H](O)[C@@H](O)C(=O)O
Reaction #969886
(5R)-5-{4-[2-(5-ethylpyridin-2-yl)ethoxy]benzyl}-1,3-thiazolidine-2,4-dione L-tartrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CCc1ccc(CCOc2ccc(C[C@H]3SC(=O)NC3=O)cc2)nc1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #969887
(5R)-5-{4-[2-(5-ethylpyridin-2-yl)ethoxy]benzyl}-1,3-thiazolidine-2,4-dione tosylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CCc1ccc(CCOc2ccc(C[C@H]3SC(=O)NC3=O)cc2)nc1.Cl
Reaction #1609976
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07
CCc1ccc(CCOc2ccc(C[C@H]3SC(=O)NC3=O)cc2)nc1.O=C(O)[C@H](O)[C@@H](O)C(=O)O
Reaction #1609977
(5R)-5-{4-[2-(5-ethylpyridin-2-yl)ethoxy]benzyl}-1,3-thiazolidine-2,4-dione L-tartrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07
CCc1ccc(CCOc2ccc(C[C@H]3SC(=O)NC3=O)cc2)nc1.Cl
Reaction #2495469
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_08
CCc1ccc(CCOc2ccc(C[C@H]3SC(=O)NC3=O)cc2)nc1.O=C(O)[C@H](O)[C@@H](O)C(=O)O
Reaction #2495470
(5R)-5-{4-[2-(5-ethylpyridin-2-yl)ethoxy]benzyl}-1,3-thiazolidine-2,4-dione L-tartrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_08
CCc1ccc(CCOc2ccc(C[C@H]3SC(=O)NC3=O)cc2)nc1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #2495471
title compound
المردود 89.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_08