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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 548560생성일: 2026년 10월 26일

4-(2-Propyn-1-yl)morpholine → (4-{3-[3-Bromo-5-(3-morpholin-4-yl-prop-1-ynyl)-phenyl]-prop-2-ynyloxy}-2-methylphenoxy)-acetic acid methyl ester

https://huagongshe.com/reaction/548560

반응식

참여 물질

역할이름HCID투입량
반응물4-(2-Propyn-1-yl)morpholineHCID 412941—
반응물{4-[3-(3,5-Dibromo-phenyl)-prop-2-ynyloxy]-2-methyl-phenoxy}-acetic acid methyl esterHCID 67157962—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매DimethylformamideHCID 6228—
용매TriethylamineHCID 8471—
생성물(4-{3-[3-Bromo-5-(3-morpholin-4-yl-prop-1-ynyl)-phenyl]-prop-2-ynyloxy}-2-methylphenoxy)-acetic acid methyl esterHCID 67157848—

반응 조건

온도60 °C

반응 단계

A mixture of 4-prop-2-ynyl-morpholine (330 mg, 2.64 mmol), {4-[3-(3,5-dibromophenyl)-prop-2-ynyloxy]-2-methyl-phenoxy}-acetic acid methyl ester (206 mg, 0.44 mmol, intermediate 2), Pd(PPh3)2Cl2 (50 mg, 0.044 mmol), CuI (23 mg, 0.123 mmol) in dry DMF (2 ml) and triethylamine (2 ml) was heated in a microwave own for 30 min at 60° C. in a sealed tube. The reaction mixture was filtered through Decalite and the filtrate was evaporated. The residue was purified on column chromatography using methylene chloride/THF mixtures to give (4-{3-[3-bromo-5-(3-morpholin-4-yl-prop-1-ynyl)-phenyl]-prop-2-ynyloxy}-2-methylphenoxy)-acetic acid methyl ester in 130 mg (58%) yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07943612B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-590996a91dd44db6befdbae9d5c61c21
출처 메모uspto-grants-2011_05