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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

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물tert-Butyl acrylateHCID 15458—
반응물7-Iodo-3-(4-phenoxyphenyl)thieno[3,2-c]pyridin-4-amineHCID 18450878—
용매DimethylformamideHCID 6228—
생성물Tert-butyl (2e)-3-[4-amino-3-(4-phenoxyphenyl)thieno[3,2-c]pyridin-7-yl]acrylateHCID 6977650561%

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온도80 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07202363B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-46c4e3b0b2fe439c8dcf2d951c6e8f1c
출처 메모uspto-grants-2007_04