Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78613생성일: 2026년 10월 23일
Potassium Carbonate → Tert butyl-5-(2-bromophenyl)-3-(5-phenyl-1,3,4-oxadiazol-2-yl)pyrazin-2-yl(tert-butoxycarbonyl)carbamate
https://huagongshe.com/ko/reaction/78613
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | (2-Bromophenyl)boronic acid | HCID 2773294 | — |
| 반응물 | Tert-butyl N-[5-bromo-3-(5-phenyl-1,3,4-oxadiazol-2-yl)pyrazin-2-yl]-N-tert-butoxycarbonyl-carbamate | HCID 59471994 | — |
| 촉매 | Palladium--triphenylphosphane (1/1) | HCID 15220664 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Tert butyl-5-(2-bromophenyl)-3-(5-phenyl-1,3,4-oxadiazol-2-yl)pyrazin-2-yl(tert-butoxycarbonyl)carbamate | HCID 59472100 | — |
반응 단계
A mixture of (2-bromophenyl)boronic acid (100 mg, 0.4979 mmol), tert-butyl N-[5-bromo-3-(5-phenyl-1,3,4-oxadiazol-2-yl)pyrazin-2-yl]-N-tert-butoxycarbonyl-carbamate (258.1 mg, 0.4979 mmol), potassium carbonate (206.5 mg, 1.494 mmol) and triphenylphosphane palladium (13.06 mg, 11.54 μL, 0.04979 mmol) in DMF (3 mL) was heated at 50° C. for 1 h. The reaction mixture was cooled to room temperature and filtered through a Celite,™ pad. The pad was washed with ethyl acetate (1×10 mL) and the combined filtrates were washed with water (2×10 mL) and brine (1×10 mL), dried over MgSO4 and concentrated to leave the product as a solid which was used directly in the next step without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08841308B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-5aa3b9cc5e2c47e9accd4c77576184eb |
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| 출처 메모 | uspto-grants-2014_09 |
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