Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 331497생성일: 2026년 10월 24일
Trifluoroacetic acid → Tert-butyl 5-[5-[3-[bis(tert-butoxycarbonyl)amino]-6-bromopyrazin-2-yl]isoxazol-3-yl]indole-1-carboxylate
https://huagongshe.com/ko/reaction/331497
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 반응물 | Iodobenzene diacetate | HCID 76724 | — |
| 반응물 | tert-butyl N-(5-bromo-3-ethynylpyrazin-2-yl)-N-[(tert-butoxy)carbonyl]carbamate | HCID 58070394 | — |
| 반응물 | HCID 88996357 | HCID 88996357 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | Tert-butyl 5-[5-[3-[bis(tert-butoxycarbonyl)amino]-6-bromopyrazin-2-yl]isoxazol-3-yl]indole-1-carboxylate | HCID 89037198 | 16.5% |
반응 단계
A solution of tert-butyl 5-((hydroxyimino)methyl)-1H-indole-1-carboxylate (260.3 mg, 1 mmol) in methanol (1 mL) was added slowly to a stirred solution of tert-butyl N-(5-bromo-3-ethynyl-pyrazin-2-yl)-N-tert-butoxycarbonyl-carbamate (438.1 mg, 1.100 mmol) and (diacetoxyiodo)benzene (354.3 mg, 1.100 mmol) in methanol (2 mL) containing trifluoroacetic acid (15 μL, 0.1947 mmol) at ambient temperature. The reaction was stirred at this temperature for 17 hours then concentrated in vacuo. The residue was purified by column chromatography (ISCO Companion, 40 g column) loaded with dichloromethane and eluted with 0 to 50% ethyl acetate/petroleum ether. Product fractions were combined and concentrate in vacuo to give the sub-title product as a white solid (108 mg, 16% Yield). 1H NMR (400.0 MHz, DMSO-d6) δ 1.22 (s, 18H), 1.57 (s, 9H), 6.73 (d, 1H), 7.69 (d, 1H), 7.80 (s, 1H), 7.89 (dd, 1H), 8.11 (d, 1H), 8.23 (d, 1H) and 8.94 (s, 1H) ppm.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08877759B2 |
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| 출처 데이터셋 | uspto-grants-2014_11 |
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| ORD ID | ord-a68360ef282b44fe8b6fd13654043420 |
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| 출처 메모 | uspto-grants-2014_11 |
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