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HRID 50640作成日:2026年10月26日

Thioglycolic Acid → 4-Methyl-2-(s)-[2-(rs)-(4-chlorophenyl)-4-oxo-thiazolidin-3-yl]-pentanoic acid methyl ester

https://huagongshe.com/reaction/50640

反応式

関与物質

役割名称HCID仕込み量
反応物Thioglycolic AcidHCID 1133—
反応物4-ChlorobenzaldehydeHCID 7726—
反応物TriethylamineHCID 8471—
反応物(+)-L-Leucine methyl esterHCID 65105—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
溶媒1,4-DioxaneHCID 31275—
生成物4-Methyl-2-(s)-[2-(rs)-(4-chlorophenyl)-4-oxo-thiazolidin-3-yl]-pentanoic acid methyl esterHCID 53711856—

反応手順

A suspension of (L)-leucine methyl ester (10 g, 55 mmol) and triethylamine (7.7 ml, 55 mmol) in 120 ml of dioxane was stirred at room temperature for 5 minutes. 3 Å molecular sieves were added followed by p-chlorobenzaldehyde (17 g, 121 mmol). The mixture was heated at 80° C. for 4 hrs. Mercaptoacetic acid (14.2 ml, 203.5 mmol) was added to the mixture and the heating was continued for an additional 12 hrs. The reaction mixture was cooled to room temperature, and diluted with ethyl acetate (40 ml) and water (30 ml). The reaction mixture was filtered to remove the molecular sieves. The organic layer was diluted with ethyl acetate (100 ml), washed twice with 60 ml of saturated solution of sodium carbonate, twice with aqueous 1N HCl and once with water. The organic layer was dried with MgSO4 and evaporated to give a residue that was carried out to the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713477B1
出典データセットuspto-grants-2004_03
ORD IDord-99910d95f2264829ac7b7cdd541f92fd
出典メモuspto-grants-2004_03