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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 962769생성일: 2026년 10월 26일

1-(2-Methoxyphenyl)piperazine → Ethyl 4-{3-{4-(4-methylphenylmethoxy)-3-{3-[4-(2-methoxyphenyl)piperazin-1-yl]propoxy}benzoyl}indol-1-yl}butanoate

https://huagongshe.com/reaction/962769

반응식

참여 물질

역할이름HCID투입량
반응물1-(2-Methoxyphenyl)piperazineHCID 1346—
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물Ethyl 4-{3-[4-(4-methylphenylmethoxy)-3-(3-chloropropoxy)benzoyl]indol-1-yl}butanoateHCID 19085526—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물Ethyl 4-{3-{4-(4-methylphenylmethoxy)-3-{3-[4-(2-methoxyphenyl)piperazin-1-yl]propoxy}benzoyl}indol-1-yl}butanoateHCID 1908553374.3%

반응 조건

온도60 °C

반응 단계

Ethyl 4-{3-[4-(4-methylphenylmethoxy)-3-(3-chloropropoxy)benzoyl]indol-1-yl}butanoate (2.59 g) obtained in Step 2 was dissolved in N,N-dimethylformamide (30 ml). 1-(2-Methoxyphenyl)piperazine (1.36 g), potassium carbonate (0.85 g), and potassium iodide (1.02 g) were added to the resultant solution and stirred overnight at 60° C. The reaction mixture was poured into water and extracted with ethyl acetate. The resultant extract was washed with brine and then dried. The solvent was distilled off. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:2), obtaining 2.47 g of ethyl 4-{3-{4-(4-methylphenylmethoxy)-3-{3-[4-(2-methoxyphenyl)piperazin-1-yl]propoxy}benzoyl}indol-1-yl}butanoate as a colorless oily substance.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05760040
출처 데이터셋uspto-grants-1998_06
ORD IDord-9a51cf912e8c45a687e1cf1e79deb12a
출처 메모uspto-grants-1998_06