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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Thioglycolic Acid | HCID 1133 | — |
| 反応物 | 4-Chlorobenzaldehyde | HCID 7726 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | (+)-L-Leucine methyl ester | HCID 65105 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 4-Methyl-2-(s)-[2-(rs)-(4-chlorophenyl)-4-oxo-thiazolidin-3-yl]-pentanoic acid methyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06713477B1 |
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| 出典データセット | uspto-grants-2004_03 |
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| ORD ID | ord-99910d95f2264829ac7b7cdd541f92fd |
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| 出典メモ | uspto-grants-2004_03 |
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