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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1916531생성일: 2026년 10월 27일

Sodium Carbonate → 5-(4-Chloro-phenyl)-2-[4-(4-pyrrolidin-1-ylmethyl-phenyl)-but-1-ynyl]-pyridine

https://huagongshe.com/reaction/1916531

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물p-Chlorophenylboric acidHCID 17810664—
반응물5-Bromo-2-[4-(4-pyrrolidin-1-ylmethyl-phenyl)-but-1-ynyl]-pyridineHCID 69071391—
용매1,4-DioxaneHCID 31275—
생성물5-(4-Chloro-phenyl)-2-[4-(4-pyrrolidin-1-ylmethyl-phenyl)-but-1-ynyl]-pyridineHCID 9978377—

반응 조건

온도100 °C

반응 단계

A mixture of 100 mg (0.27 mmol) 5-bromo-2-[4-(4-pyrrolidin-1-ylmethyl-phenyl)-but-1-ynyl]-pyridine, 85 mg (0.54 mmol) 4-chloro-phenylboric acid, 15.7 mg (0.014 mmol) tetrakis-triphenylphosphane-palladium, 0.28 mL of a 2 M aqueous Na2CO3 solution in 10 mL 1,4-dioxane is heated for 8 h at 100° C. under an argon atmosphere. The solvent is distilled off i.vac., the residue is taken up in water, exhaustively extracted with EtOAc and dried over Na2SO4. After the desiccant and solvent have been eliminated the residue is purified over neutral Alox (ICN Alumina N+5% H2O; cyc/EtOAc 7:3). The product fractions are evaporated down, the residue is triturated with PE and suction filtered.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08618132B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-a3a109de35a44f07b79f23a3caddfcf8
출처 메모uspto-grants-2013_12