참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Acrylate | HCID 8821 | — |
| 반응물 | Tri-o-tolylphosphine | HCID 80271 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 2-Amino-5-bromo-4-methylpyridine | HCID 817695 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 용매 | Propionitrile | HCID 7854 | — |
| 생성물 | Ethyl (E)-3-(6-amino-4-methylpyridin-3-yl)acrylate | HCID 57440845 | 59% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07557125B2 |
|---|
| 출처 데이터셋 | uspto-grants-2009_07 |
|---|
| ORD ID | ord-11ef8d546f2942e882ed85f1ac542b6a |
|---|
| 출처 메모 | uspto-grants-2009_07 |
|---|