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HRID 882706作成日:2026年10月27日

(E)-5-(4-(2-(5-ethylpyridin-2-yl)ethoxy)benzylidene)thiazolidine-2,4-dione → Pioglitazone, (R)-

https://huagongshe.com/reaction/882706

反応式

関与物質

役割名称HCID仕込み量
反応物(E)-5-(4-(2-(5-ethylpyridin-2-yl)ethoxy)benzylidene)thiazolidine-2,4-dioneHCID 14211277—
溶媒EthanolHCID 702—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物Pioglitazone, (R)-HCID 29010894—

反応手順

A stock solution of the Rh(COD)2BF4 (10.6 mg, 26.1 μmol) in DCM (9.5 mL) was made in a glove box. Ligand SL-WO03-2 ((S)-1-[(S)-2-(2i -diphenylphosphinophenyl)ferrocenyl]ethyl-dicyclohexyl phosphine) (8.4 mg, 12.5 μmol), was weighed into a vial and 500 μL of the Rh(COD)2BF4 stock solution was added. A solution of 5-[1-{4-[2-(5-ethyl-pyridin-2-yl)-ethoxy]-phenyl}-meth-(E)-ylidene]-thiazolidine-2,4-dione (4.5 mL of a stock solution containing 78.2 mg in 35 mL MeOH) was added to the reaction vial containing the catalyst solution. The vial was purged with N2 (5×) and H2 (5×) and finally charged with 25 bar of H2. After 18 h the H2 was released and the reaction vial was purged with N2 (3×). A sample of the reaction vial was taken and diluted with an equal volume of EtOH containing 1% formic acid. e.e. (Method 4) 75%, Rt 36.11 min, conversion 50%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08236786B2
出典データセットuspto-grants-2012_08
ORD IDord-bce85533d58a4772baa668753a77e8e5
出典メモuspto-grants-2012_08