Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1270841생성일: 2026년 10월 26일
Triethylamine → Tert-butyl (2e)-3-[4-amino-3-(4-phenoxyphenyl)thieno[3,2-c]pyridin-7-yl]acrylate
https://huagongshe.com/reaction/1270841
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | tert-Butyl acrylate | HCID 15458 | — |
| 반응물 | 7-Iodo-3-(4-phenoxyphenyl)thieno[3,2-c]pyridin-4-amine | HCID 18450878 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Tert-butyl (2e)-3-[4-amino-3-(4-phenoxyphenyl)thieno[3,2-c]pyridin-7-yl]acrylate | HCID 69776505 | 61% |
반응 단계
A mixture of Example 10B (0.417 g, 0.94 mmol), tert-butyl acrylate (0.26 mL, 1.74 mol) and triethylamine (0.7 mL, 5 mmol) in DMF (3 mL) was degassed with nitrogen for 45 minutes, treated with PdCl2(o-tol3P)2 (0.032 g, 0.046 mmol), and heated to 80° C. overnight. The resulting mixture was cooled to room temperature, then partitioned between water and ethyl acetate. The organic extract was washed with brine, dried (Na2SO4), filtered, and concentrated. The residue was purified by flash column chromatography on silica gel with 30% ethyl acetate/hexanes to provide 0.25 g (61% yield) of the desired product. MS (ESI(+)) m/e 445 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07202363B2 |
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| 출처 데이터셋 | uspto-grants-2007_04 |
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| ORD ID | ord-46c4e3b0b2fe439c8dcf2d951c6e8f1c |
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| 출처 메모 | uspto-grants-2007_04 |
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