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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073548Generated: October 30, 2026

Methyl iodide → Methyl 4-[5-(N-cyclopentylmethylcarbamoyl)-1-methylindol-3-ylmethyl]-3-methoxybenzoate

https://huagongshe.com/reaction/2073548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactantmethyl 4-[5-(N-cyclopentylmethylcarbamoyl)indol-3-ylmethyl]-3-methoxybenzoateHCID 10070759—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-[5-(N-cyclopentylmethylcarbamoyl)-1-methylindol-3-ylmethyl]-3-methoxybenzoateHCID 1007160255%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of methyl 4-[5-(N-cyclopentylmethylcarbamoyl)indol-3-ylmethyl]-3-methoxybenzoate (C) (1.52 g) in N,N-dimethylformamide (5 ml) was added to a slurry of sodium hydride (0.088 g) in N,N-dimethylformamide (3 ml) at 0° C. The mixture was stirred under a nitrogen atmosphere for 20 minutes at 0° C. and for 15 minutes at 25° C. The reaction was cooled to 0° C., treated with a cold solution of iodomethane (0.57 g) in N,N-dimethylformamide (2 ml), and then allowed to warm to 25°. The mixture was recooled to 0°, quenched with saturated aqueous ammonium chloride, and evaporated. The residue was dissolved in ethyl acetate, washed with water and brine, dried (MgSO4), and evaporated. The amber residue was purified by flash chromatography on silica gel (500 ml), eluting with 1:9 v/v ethyl acetate:chloroform, to yield the title compound (0.86 g, 55%) as a white foam; partial NMR (80 MHz, CDCl 3): 3.4(dd, 2H, CH2N), 3.73(s, 3H, NCH3), 3.89(s, 3H, OCH3), 3.92(s, 3H, OCH3), 4.12(s, 2H, ArCH2), 6.11(t, 1H, NH), 6.8(s, 1H, H2 -indole), 8.00(br s, 1H, H4 -indole).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04918094
Source datasetuspto-grants-1990_04
ORD IDord-c6c986557e1e4e69a60c15bebdf76de5
Source noteuspto-grants-1990_04