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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1916722생성일: 2026년 10월 26일

Triphenylphosphine → 5-(4-Chloro-phenyl)-2-[3-(4-pyrrolidin-1-ylmethyl-phenoxy)-prop-1-ynyl]-pyridine

https://huagongshe.com/reaction/1916722

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물4-(Pyrrolidin-1-ylmethyl)phenolHCID 18771978—
반응물3-[5-(4-Chloro-phenyl)-pyridin-2-yl]-prop-2-yn-1-olHCID 69076337—
용매TetrahydrofuranHCID 8028—
생성물5-(4-Chloro-phenyl)-2-[3-(4-pyrrolidin-1-ylmethyl-phenoxy)-prop-1-ynyl]-pyridineHCID 59835746—

반응 단계

131 mg (0.5 mmol) triphenylphosphane are added to a solution of 100 mg (0.41 mmol) 3-[5-(4-chloro-phenyl)-pyridin-2-yl]-prop-2-yn-1-ol and 88 mg (0.5 mmol) 4-pyrrolidin-1-ylmethyl-phenol in 4 mL THF. Then 0.1 mL (0.5 mmol) diisopropyl azo-dicarboxylate is slowly added dropwise and the reaction mixture is stirred for 3 h at RT. The mixture is evaporated down i. vac., the residue is taken up in 1 mL DMF and purified by HPLC. The product obtained, which still contains triphenylphosphane oxide, is again purified by chromatography (silica gel, EtOAc after EtOAc/MeOH/NH3 9:1:0.1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08618132B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-f08aa4f833cf41098db3611a2b4d8708
출처 메모uspto-grants-2013_12