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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904472Generated: October 30, 2026

1,1'-Carbonyldiimidazole → Methyl 4-[6-(2-cyclopentylacetamido)indol-1-ylmethyl]-3-methoxybenzoate

https://huagongshe.com/reaction/1904472

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantCyclopentylacetic acidHCID 71606—
ReactantMethyl 4-(6-aminoindol-1-ylmethyl)-3-methoxybenzoateHCID 14708762—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-[6-(2-cyclopentylacetamido)indol-1-ylmethyl]-3-methoxybenzoateHCID 19744328—

Reaction Steps

A solution of cyclopentylacetic acid (0.24 ml) and 1,1'-carbonyldiimidazole (0.34 g) in methylene chloride (3 ml) was heated under reflux for 30 minutes and then treated with a solution of ester (B) (0.5 g) in methylene chloride (3 ml). The mixture was heated under reflux for 30 minutes, stirred at room temperature for 24 hours, and then diluted with ethyl acetate. This organic solution was washed sequentially with 10% v/v hydrochloric acid, water, and brine, dried (MgSO4) and evaporated. The residue was purified by flash chromatography on a 6×18 cm silica gel column using 99:1 v/v ethyl acetate:toluene as the eluent followed by recrystallization from hexane/ethyl acetate to give methyl 4-[6-(2-cyclopentylacetamido)indol-1-ylmethyl]-3-methoxybenzoate (P) as a solid; partial NMR: 2.0-2.5(br m, 3H, CH2CH), 3.9(s, 3H, OCH3), 4.0(s, 3H, OCH3), 5.3(s, 2H, NCH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04837235
Source datasetuspto-grants-1989_06
ORD IDord-370fdd4173bc478f83061eb0575925a1
Source noteuspto-grants-1989_06