Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 520487생성일: 2026년 10월 24일
Ethyl 2-((tert-butoxycarbonyl)amino)-1,3-thiazole-4-carboxylate → (4-Hydroxymethylthiazol-2-yl)carbamic acid tert-butyl ester
https://huagongshe.com/ko/reaction/520487
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl 2-((tert-butoxycarbonyl)amino)-1,3-thiazole-4-carboxylate | HCID 22280595 | — |
| 반응물 | Lithium triethylborohydride | HCID 23712863 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Acetonitrile dry ice | HCID 86587134 | — |
| 생성물 | (4-Hydroxymethylthiazol-2-yl)carbamic acid tert-butyl ester | HCID 22280475 | 72% |
반응 단계
Ethyl 2-(tert-butoxycarbonylamino)thiazole-4-carboxylate 88 (10.5 g, 38.6 mmol) was dissolved in 300 mL of anhydrous THF and cooled in dry ice-acetonitrile bath. A solution of 1 M Super Hydride™ in THF (85 mL) was then added over a period of 10 min. The resulting reaction mixture was stirred at −45° C. for 2 h. Another portion of 1 M Super Hydride™ in THF (35 mL) was then added and the reaction mixture was stirred for an additional 2 h at −45° C. The reaction was quenched at −45° C. by the addition of 50 mL of brine. Upon warming to room temperature, the reaction mixture was concentrated under reduced pressure. The resulting mixture was extracted with EtOAc. The combined organic layers were washed with brine, dried with Na2SO4, and concentrated under reduced pressure. The resulting residue was purified by chromatography to afford 89 (6.39 g, 72% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09326986B2 |
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| 출처 데이터셋 | uspto-grants-2016_05 |
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| ORD ID | ord-10a357909e524ca49f2be272cb2ef0ee |
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| 출처 메모 | uspto-grants-2016_05 |
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