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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2363434생성일: 2026년 10월 26일

7,12-Dimethylbenz(a)anthracene → 1-[2-(3,5-Dichloro-4-hydroxy-benzoylamino)-propionyl]-pyrrolidine-2-carboxylic acid (2-ethoxy-5-oxo-tetrahydro-furan-3-yl)-amide

https://huagongshe.com/reaction/2363434

반응식

참여 물질

역할이름HCID투입량
반응물7,12-Dimethylbenz(a)anthraceneHCID 6001—
반응물Dichloromethane methanolHCID 21226129—
반응물1-[2-(4-Allyloxy-3,5-dichloro-benzoylamino)-propionyl]-pyrrolidine-2-carboxylic acid (2-ethoxy-5-oxo-tetrahydro-furan-3-yl)-amideHCID 22977487—
촉매HCID 178418397HCID 178418397—
용매DichloromethaneHCID 6344—
생성물1-[2-(3,5-Dichloro-4-hydroxy-benzoylamino)-propionyl]-pyrrolidine-2-carboxylic acid (2-ethoxy-5-oxo-tetrahydro-furan-3-yl)-amideHCID 2297746377%

반응 단계

To a solution of 110 (1.94 mg, 0.36 mmol) in CH2Cl2 (5 ml) was added DMBA (70.7 mg, 0.45 mmol) and Pd(PPh3)4 (50.3 mg, 0.044 mmol) at 0° C. The solution was warmed to room temperature after 15 mins, stirred for 2 hours, diluted with CH2Cl2 then washed with water (2×) and brine. The organic layer was dried over anhydrous Na2SO4 and evaporated to give the crude product. Flash chromatography using CH2Cl2/MeOH (99/1 to 95/5%) afforded the title compound (138.6 mg, 77% yield). 1H-NMR (500 MHz, CD3OD) δ 1.13-1.31 (m, 3H), 1.35-1.49 (m, 3H), 1.84-2.35 (m, 4H), 2.43-3.0.5 (m, 2H) 3.48-3.93 (m, 4H), 4.22-4.80 (m, 3H), 5.38 (d, 0.4H), 5.46 (s, 0.1H), 5.55-5.61 (m, 0.5H), 7.76-7.94 (m, 2H). Analytical HPLC 8.70 min. LC-MS (ES+) m/e=502.2 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08691848B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-0a408391f5ce4aa5817ad07c8a3cfab8
출처 메모uspto-grants-2014_04