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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392193Generated: October 30, 2026

Benzyl Bromide → 1-Benzyl-4-[3-methyl-1-(3-phenyl-propyl)-1H-indole-6-yl]-pyrrolidine-2-one

https://huagongshe.com/reaction/392193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
Reactant4-[3-methyl-1-(3-phenyl-propyl)-1H-indole-6-yl]-pyrrolidine-2-oneHCID 22663451—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-4-[3-methyl-1-(3-phenyl-propyl)-1H-indole-6-yl]-pyrrolidine-2-oneHCID 2266330477.5%

Reaction Steps

A solution of sodium hydride (0.013 g) in tetrahydrofuran at 0° C., under argon, was treated with a solution of 4-[3-methyl-1-(3-phenyl-propyl)-1H-indole-6-yl]-pyrrolidine-2-one (0.184 g, Example 20) and benzyl bromide (0.094 g) in dry tetrahydrofuran. The mixture was allowed to warm to room temperature then treated with N,N′-dimethylpropyleneurea (0.05 g). After stirring at room temperature overnight the solution was partitioned between ethyl acetate (15 ml)and 1N hydrochloric acid (15 ml). The organic phase was dried over magnesium sulphate then evaporated. The residue was subjected to preparative layer chromatography on silica using a mixture of ethyl acetate and hexane (3:7, v/v) as eluent to yield the title compound (0.18 g) as an oil. [Elemental analysis:— C, 79.16; H, 6.98; N, 6.14%. Calculated for C29H30N2O.H2O:— C, 79.04; H, 7.33; N, 6.36%].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800645B1
Source datasetuspto-grants-2004_10
ORD IDord-3e43a644194c4e91a83ad9b68f7b1a6a
Source noteuspto-grants-2004_10