Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50640생성일: 2026년 10월 26일
Thioglycolic Acid → 4-Methyl-2-(s)-[2-(rs)-(4-chlorophenyl)-4-oxo-thiazolidin-3-yl]-pentanoic acid methyl ester
https://huagongshe.com/reaction/50640
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Thioglycolic Acid | HCID 1133 | — |
| 반응물 | 4-Chlorobenzaldehyde | HCID 7726 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | (+)-L-Leucine methyl ester | HCID 65105 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 4-Methyl-2-(s)-[2-(rs)-(4-chlorophenyl)-4-oxo-thiazolidin-3-yl]-pentanoic acid methyl ester | HCID 53711856 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06713477B1 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-99910d95f2264829ac7b7cdd541f92fd |
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| 출처 메모 | uspto-grants-2004_03 |
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