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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 728673생성일: 2026년 10월 25일

Methyl 4-(bromomethyl)-3-methoxybenzoate → Methyl 4-[1-(2-carbamoylethyl)-5-(N-cyclopentylmethylcarbamoyl)indol-3-ylmethyl]-3-methoxybenzoate

https://huagongshe.com/reaction/728673

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참여 물질

역할이름HCID투입량
반응물Methyl 4-(bromomethyl)-3-methoxybenzoateHCID 2759828—
반응물1-(2-carbamoylethyl)-5-(N-cyclopentylmethylcarbamoyl)indoleHCID 19822477—
촉매HCID 178418778HCID 178418778—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물Methyl 4-[1-(2-carbamoylethyl)-5-(N-cyclopentylmethylcarbamoyl)indol-3-ylmethyl]-3-methoxybenzoateHCID 1982247339%

반응 조건

온도80 °C

반응 단계

Silver(I) oxide (0.17 g) was added to a solution of 1-(2-carbamoylethyl)-5-(N-cyclopentylmethylcarbamoyl)indole (0.70 g) and methyl 4-bromomethyl-3-methoxybenzoate (B)(0.19 g) in 1,4-dioxane (10 ml). The mixture was protected from light and stirred at 80° C. under an atmosphere of nitrogen for 12 hours. The mixture was then diluted with 1:1 v/v ethyl acetate:ether (50 ml) and filtered. The filtrate was washed sequentially with water and brine, dried (MgSO4), and evaporated. The residual yellow gum was purified by flash chromatography on silica gel (500 ml), eluting with 5:95 v/v methanol:chloroform to give the title compound (0.14 g, 39%) as a white solid; mp 189°-191° C. (d); NMR (250 MHz, DMSO-d6): 1.2-1.8(broad m, 8H, cyclopentyl), 2.2(sep, 1H, cyclopentylmethine), 3.2(t, 2H, CH2NH), 7.2(m, 2H), 7.3(broad s, 1H, CONH2), 7.5 (m, 3H), 7.7(d, 1H, H6 -indole), 8.0(s, 1H, H4 -indole), 8.3(t, 1H, NHCO).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05049679
출처 데이터셋uspto-grants-1991_09
ORD IDord-52361734dd5344259ca8db06edd05715
출처 메모uspto-grants-1991_09