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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073543Generated: October 25, 2026

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

https://huagongshe.com/reaction/2073543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-(bromomethyl)-3-methoxybenzoateHCID 2759828—
Reactant1-(2-carbamoylethyl)-5-(N-cyclopentylmethylcarbamoyl)indoleHCID 19822477—
CatalystHCID 178418778HCID 178418778—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 4-[1-(2-carbamoylethyl)-5-(N-cyclopentylmethylcarbamoyl)indol-3-ylmethyl]-3-methoxybenzoateHCID 1982247339%

Reaction Conditions

Temperature80 °C

Reaction Steps

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):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04918094
Source datasetuspto-grants-1990_04
ORD IDord-96ba4228451b40faa5514bcf3b88ac14
Source noteuspto-grants-1990_04