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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1095026생성일: 2026년 10월 27일

Cesium carbonate → Benzo[1,3]dioxol-4-yl-(2-chloro-5-methyl-pyrimidin-4-yl)-amine

https://huagongshe.com/reaction/1095026

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
반응물4-Bromo-1,3-benzodioxoleHCID 2776189—
반응물2-Chloro-5-methylpyrimidin-4-amineHCID 4302175—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매DichloromethaneHCID 6344—
용매1,4-DioxaneHCID 31275—
생성물Benzo[1,3]dioxol-4-yl-(2-chloro-5-methyl-pyrimidin-4-yl)-amineHCID 5767494639.1%

반응 단계

A mixture of 2-chloro-5-methyl-pyrimidin-4-ylamine (1.4 g, 9.7 mmol), 4-bromo-benzo[1,3]dioxole (2.0 g, 10 mmol), Pd2(dba)3 (0.80 g, 0.87 mmol), Xantphos (1.0 g, 1.7 mmol) and cesium carbonate (6.3 g, 19 mmol) was suspended in dioxane (40 mL) and heated at reflux under the argon atmosphere for 5 h. The reaction mixture was cooled to room temperature and diluted with DCM (30 mL). The mixture was filtered and the filtrate concentrated in vacuo. The residue was purified by flash chromatography on silica gel (hexanes to 50% EtOAc/hexanes) to afford the title compound (1.0 g, 39%) as a white solid. 1H NMR (500 MHz, DMSO-d6): δ 2.13 (s, 3H), 5.99 (s, 2H), 6.80-6.90 (m, 3H), 8.01 (s, 1H), 8.92 (s, 1H). MS (ES+): m/z 264 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08133900B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-25da4c06c72947c9a012a8d42f245bac
출처 메모uspto-grants-2012_03