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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728681Generated: October 26, 2026

Methyl 4-(bromomethyl)-3-methoxybenzoate → methyl 4-[5-[N-(3-methylbutyl)carbamoyl]indol-3-ylmethyl]-3-methoxybenzoate

https://huagongshe.com/reaction/728681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-(bromomethyl)-3-methoxybenzoateHCID 2759828—
Reactant5-[N-(3-methylbutyl)carbamoyl]-indoleHCID 9991466—
CatalystHCID 178418778HCID 178418778—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Productmethyl 4-[5-[N-(3-methylbutyl)carbamoyl]indol-3-ylmethyl]-3-methoxybenzoateHCID 1036410613%

Reaction Steps

Silver(I) oxide (4.92 g) was added to a solution of indole (F) (2.05 g) in toluene (15 ml). The mixture was protected from light, stirred, and heated to reflux under an atmosphere of nitrogen for 24 hours. A solution of methyl 4-bromomethyl-3-methoxybenzoate (B) (2.31 g) in toluene (5 ml) was added, and stirring was continued at 95° C. for 4 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 (862 ml), eluting with 1:99 v/v methanol:chloroform to give (E) (0.47 g, 13%) as a white foam; partial NMR (80 MHz, CDCl3): 0.92[d, 6H, CH(CH3)2], 3.40(q, 2H, NCH2), 3.87(s, 3H, OCH3), 4.09(s, 2H, ArCH2), 6.18(br t, 1H, CONH), 7.98(br s, 1H, H4 -indole), 8.84(br s, 1; H, NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05049679
Source datasetuspto-grants-1991_09
ORD IDord-1aecf0972f2d4a63ba3cefa1d2bfc937
Source noteuspto-grants-1991_09