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HRID 728682作成日:2026年10月25日

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

https://huagongshe.com/reaction/728682

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 4-(bromomethyl)-3-methoxybenzoateHCID 2759828—
反応物5-[N-(cyclopentylmethyl)-N-methylcarbamoyl]-1-methylindoleHCID 19822471—
触媒HCID 178418778HCID 178418778—
溶媒Ethyl AcetateHCID 8857—
溶媒1,4-DioxaneHCID 31275—
生成物Methyl 4-[5-[N-(cyclopentylmethyl)-N-methylcarbamoyl]-1-methylindol-3-ylmethyl]-3-methoxybenzoateHCID 1982247213.2%

反応手順

Silver(I) oxide (0.30 g) was added to a solution of 5-[N-(cyclopentylmethyl)-N-methylcarbamoyl]-1-methylindole (G) (0.35 g) in dioxane (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 additional 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, NCH2), 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05049679
出典データセットuspto-grants-1991_09
ORD IDord-c9fe621e7a3342c48fd04c1ea3b4ba1b
出典メモuspto-grants-1991_09