反応式
C([C:3]1([C:11]2[CH:16]=[C:15]([OH:17])[CH:14]=[CH:13][C:12]=2[OH:18])[NH:7][CH:6]([C:8]([O-:10])=[O:9])[CH2:5][S:4]1)C.Cl.N[C@H:21](C(O)=O)CS>>[OH:18][C:12]1[CH:13]=[CH:14][C:15]([OH:17])=[CH:16][C:11]=1[CH:3]1[NH:7][CH:6]([C:8]([O:10][CH3:21])=[O:9])[CH2:5][S:4]1参加物
3
実験手順
The procedure described below for preparation of ethyl-(2,5-dihydroxyphenyl)-1,3-thiazolidine-4-carboxylate (7) was employed to make 6, except the methyl ester of L-cysteine hydrochloride was employed as starting material.
出典と根拠
- ORDレコード
- ord-f37da166f1014f5c9371b02ae8ec0e7f
- 出典データセット
- uspto-grants-2002_03
- 特許番号
- US06355661B1
関連ノート
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