돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 225883생성일: 2026년 10월 23일

Ethyl Acrylate → Ethyl (E)-3-(6-amino-4-methylpyridin-3-yl)acrylate

https://huagongshe.com/ko/reaction/225883

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcrylateHCID 8821—
반응물Tri-o-tolylphosphineHCID 80271—
반응물DiisopropylethylamineHCID 81531—
반응물2-Amino-5-bromo-4-methylpyridineHCID 817695—
촉매palladium(II) acetateHCID 167845—
용매PropionitrileHCID 7854—
생성물Ethyl (E)-3-(6-amino-4-methylpyridin-3-yl)acrylateHCID 5744084559%

반응 단계

To a stirred solution of 2-amino-5-bromo-4-methylpyridine (10 g, 54 mmole) in propionitrile (50 mL) was added ethyl acrylate (17 mL, 157 mmole), DIEA (19 mL, 106 mmole), palladium(II) acetate (0.61 g, 2.7 mmole) and tri-o-tolylphosphine (1.64 g, 5.4 mmole). The reaction was purged with argon and heated at reflux for 6 hr, then was cooled to RT and concentrated to dryness under vacuum. The resulting residue was taken up in ethyl acetate and filtered through a pad of silica gel. The filtrate was concentrated and the remaining residue was triturated with 1:1 Et2O/petroleum ether (50 mL), filtered, and dried under vacuum to give the title compound (6.50 g, 59%) as a pale yellow solid: 1H NMR (400 MHz, DMSO-d6) δ 8.31 (s, 1 H), 7.66 (d, J=16.0 Hz, 1 H), 6.40 (br s, 2 H), 6.32 (d, J=16.0 Hz, 1 H), 6.28 (s, 1 H), 4.15 (q, 2 H), 2.24 (s, 3 H), 1.24 (t, 3 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557125B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-11ef8d546f2942e882ed85f1ac542b6a
출처 메모uspto-grants-2009_07