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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2073552생성일: 2026년 10월 25일

Methyl 4-(bromomethyl)-3-methoxybenzoate → Methyl 4-[5-[N-(cyclopentylmethyl)-N-methylcarbamoyl]-1-methylindol-3-ylmethyl]-3-methoxybenzoate

https://huagongshe.com/reaction/2073552

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 4-(bromomethyl)-3-methoxybenzoateHCID 2759828—
반응물5-[N-(cyclopentylmethyl)-N-methylcarbamoyl]-1-methylindoleHCID 19822471—
촉매HCID 178418778HCID 178418778—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물Methyl 4-[5-[N-(cyclopentylmethyl)-N-methylcarbamoyl]-1-methylindol-3-ylmethyl]-3-methoxybenzoateHCID 1982247213.2%

반응 단계

Silver(I) oxide (0.30 g) was added to a solution of 5-[N-(cyclopentylmethyl)-N-methylcarbamoyl]-1-methylindole (G) (0.35 g) in dixoane (2 ml). The mixture was protected from light, stirred, and heated to reflux under an atmosphere of nitrogen for 2 hours. A solution of methyl 4-bromomethyl-3-methoxybenzoate (B) (0.33 g) in dioxane (1 ml) was added and the mixture was heated to reflux for an additonal 18 hours. The mixture was then diluted with ethyl acetate and filtered. The filtrate was evaporated to give an amber gum which was purified by flash chromatography on silica gel (223 ml), eluting with chloroform to give the title compound (75.2 mg, 13%) as a white foam; partial nmr (80 MHz, CDCl3): 3.01(s, 3H, CONCH3), 3.51(br d, 2H, HCH2), 3.74(s, 3H, NCH3), 3.89(s, 3H, OCH3), 3.92(s, 3H, OCH3), 4.10(s, 2H, ArCH2), 6.81(s, 1H, H2 -indole).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04918094
출처 데이터셋uspto-grants-1990_04
ORD IDord-a2e8b2d0524445e39da427fe277993d0
출처 메모uspto-grants-1990_04