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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

반응식

참여 물질

역할이름HCID투입량
반응물(s)-2-Mercaptosuccinic acidHCID 3246154—
반응물HCID 178444768HCID 178444768—
용매TolueneHCID 1140—
생성물2-((5S)-2-(2-(1-(tert-butoxycarbonyl)piperidin-4-yl)thiazol-5-yl)-3-(3,3-dimethylbutyl)-4-oxothiazolidin-5-yl)acetic acidHCID 57774368100.3%

반응 조건

온도110 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08163737B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-541d5c5071f141bc96b2c727b1749d81
출처 메모uspto-grants-2012_04