Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1695923생성일: 2026년 10월 26일
(s)-2-Mercaptosuccinic acid → 2-((5S)-2-(2-(1-(tert-butoxycarbonyl)piperidin-4-yl)thiazol-5-yl)-3-(3,3-dimethylbutyl)-4-oxothiazolidin-5-yl)acetic acid
https://huagongshe.com/reaction/1695923
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (s)-2-Mercaptosuccinic acid | HCID 3246154 | — |
| 반응물 | HCID 178444768 | HCID 178444768 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 2-((5S)-2-(2-(1-(tert-butoxycarbonyl)piperidin-4-yl)thiazol-5-yl)-3-(3,3-dimethylbutyl)-4-oxothiazolidin-5-yl)acetic acid | HCID 57774368 | 100.3% |
반응 단계
A mixture of (Z)-tert-butyl 4-(5-((3,3-dimethylbutylimino)methyl)thiazol-2-yl)piperidine-1-carboxylate (290 mg, 0.76 mmol, 1 eq) and (S)-2-mercaptosuccinic acid (138 mg, 0.92 mmol, 1.2 eq) in toluene (20 mL) was heated at 110° C. for 18 hr. The excess solvent was concentrated in vacuo and the solids were collected by filtration. The solids were washed with water, toluene and dried to give 2-((5S)-2-(2-(1-(tert-butoxycarbonyl)piperidin-4-yl)thiazol-5-yl)-3-(3,3-dimethylbutyl)-4-oxothiazolidin-5-yl)acetic acid (390 mg, 90% yield). (M+1) 512. 1H NMR (CDCl3) δ 7.15 (m, 1H), 5.68 (m, 1H), 4.58-4.11 (m, 3H), 3.62 (m, 1H), 3.39-3.09 (m, 2H), 2.93-2.74 (m, 3H), 2.09 (m, 2H), 1.71-1.64 (m, 2H), 1.47 (s, 9H), 1.44 (m, 1H), 0.85 (s, 9H) ppm.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08163737B2 |
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| 출처 데이터셋 | uspto-grants-2012_04 |
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| ORD ID | ord-541d5c5071f141bc96b2c727b1749d81 |
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| 출처 메모 | uspto-grants-2012_04 |
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