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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 549603생성일: 2026년 10월 25일

4-(2-Propyn-1-yl)morpholine → {4-[3-[2-(4-Chloro-phenyl)-ethoxy]-5-(3-morpholin-4-yl-prop-1-ynyl)phenylsulfanyl]-2-methyl-phenoxy}-acetic Acid Ethyl Ester

https://huagongshe.com/reaction/549603

반응식

참여 물질

역할이름HCID투입량
반응물4-(2-Propyn-1-yl)morpholineHCID 412941—
반응물(4-{3-Bromo-5-[2-(4-chloro-phenyl)-ethoxy]-phenylsulfanyl}-2-methyl-phenoxy)acetic acid ethyl esterHCID 57791905—
촉매Copper iodideHCID 83717—
촉매Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
용매DimethylformamideHCID 6228—
용매TriethylamineHCID 8471—
생성물{4-[3-[2-(4-Chloro-phenyl)-ethoxy]-5-(3-morpholin-4-yl-prop-1-ynyl)phenylsulfanyl]-2-methyl-phenoxy}-acetic Acid Ethyl EsterHCID 67171037—

반응 단계

(4-{3-Bromo-5-[2-(4-chloro-phenyl)-ethoxy]-phenylsulfanyl}-2-methyl-phenoxy)acetic acid ethyl ester (300 mg; 0.56 mmol), 4-prop-2-ynyl-morpholine (280.4 mg; 2.2 mmol), bis(triphenylphosphine) palladium (II) chloride (31.4 mg; 0.045 mmol) and copper iodide (6.4 mg; 0.034 mmol) were dissolved in a mixture of triethylamine (2 mL) and DMF (2 mL) under an atmosphere of nitrogen. The reaction mixture was reacted in a microwave oven at 110° C. for 1.5 h. The reaction mixture was evaporated to dryness, and 5% aqueous citric acid (30 mL) and ethyl acetate (30 mL) was added. The two phases were separated and the aqueous phase was extracted with ethyl acetate (30 mL). The combined organic phases were dried and evaporated to dryness and purified by preparative HPLC (method B). Yield: 300 mg; 92%. HPLC-MS: m/z: 580.7 (M+H)+; Rt: 2.16 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07943669B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-afae62dccfd641a9a5c238b09d80d5e0
출처 메모uspto-grants-2011_05