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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 273503생성일: 2026년 10월 26일

Cesium carbonate → [7-(2-Chloro-5-methoxy-phenyl)-6-methyl-benzo[1,2,4]triazin-3-yl]-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-amine

https://huagongshe.com/reaction/273503

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참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물N-(2-(p-bromophenoxy)ethyl)pyrrolidineHCID 70657—
반응물1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
반응물7-(2-Chloro-5-methoxy-phenyl)-6-methyl-benzo[1,2,4]triazin-3-ylamineHCID 68979661—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매1,4-DioxaneHCID 31275—
생성물[7-(2-Chloro-5-methoxy-phenyl)-6-methyl-benzo[1,2,4]triazin-3-yl]-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-amineHCID 59837634—

반응 조건

온도100 °C

반응 단계

7-(2-chloro-5-methoxy-phenyl)-6-methyl-benzo[1,2,4]triazin-3-ylamine (0.67 mmol, 1.0 equiv), 1-[2-(4-bromophenoxy)-ethyl] pyrrolidine (0.005 mmol, 1.5 equiv), Cs2CO3 (2.01 mmol, 3.0 equiv), Pd2(dba)3 (0.067 mmol, 0.1 equiv), and Xantphos (0.134 mmol, 0.2 equiv) were dissolved in 20 mL dioxane, placed under an argon atmosphere and refluxed at 100° C. for 18 h. The reaction was cooled to room temperature and filtered. The filtrate was dissolved in EtOAc, washed with saturated NaHCO3 and brine and organic phase was dried (Na2SO4). The organics were concentrated under reduced pressure to afford residue that was precipitated out using EtOAc/hexanes (1:5 v/v) to give [7-(2 chloro-5-methoxy-phenyl)-6-methyl-benzo[1,2,4]triazin-3-yl]-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-amine, as an orange solid (271.2 mg, 83% yield). Rf=0.56 (9:1 DCM/MeOH). MS (ES+) m/z=491. LC retention time 2.72 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456176B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-9b9cd78048554376944da750711c46d3
출처 메모uspto-grants-2008_11