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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727412Generated: November 1, 2026

2-Bromo-1-(3,4,5-trimethoxyphenyl)ethanone → N,N-diisobutyl-1-{3-[methyl(2-pyridin-2-ylethyl)amino]propyl}-2-{[2-oxo-2-(3,4,5-trimethoxyphenyl)ethyl]thio}-1H-benzimidazole-5-carboxamide

https://huagongshe.com/reaction/1727412

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1-(3,4,5-trimethoxyphenyl)ethanoneHCID 3685732—
ReactantN,N-diisobutyl-1-{3-[methyl(2-pyridin-2-ylethyl)amino]propyl}-2-thioxo-2,3-dihydro-1H-benzimidazole-5-carboxamideHCID 86596757—
SolventTetrahydrofuranHCID 8028—
ProductN,N-diisobutyl-1-{3-[methyl(2-pyridin-2-ylethyl)amino]propyl}-2-{[2-oxo-2-(3,4,5-trimethoxyphenyl)ethyl]thio}-1H-benzimidazole-5-carboxamideHCID 57567654—

Reaction Conditions

Temperature20 °C

Reaction Steps

Morpholinomethylpolystyrene resin (acquired from Novabiochem, 2 eq) and 2-bromo-1-(3,4,5-trimethoxyphenyl)ethanone are added successively to a solution of N,N-diisobutyl-1-{3-[methyl(2-pyridin-2-ylethyl)amino]propyl}-2-thioxo-2,3-dihydro-1H-benzimidazole-5-carboxamide in tetrahydrofuran. The mixture is stirred for 15 hours at approximately 20° C. then tetrahydrofuran, aminomethylpoystyrene resin (2 eq, acquired from Novabiochem) and 4-bromomethylphenoxymethyl-polystyrene resin (3 eq, acquired from Novabiochem) are added. After stirring for 6 hours, the mixture is filtered on frit. The filtrate is then concentrated to dryness under reduced pressure at 40° C. in order to produce the expected compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495110B2
Source datasetuspto-grants-2009_02
ORD IDord-b969e21ea45147678e57fdf0f98af97e
Source noteuspto-grants-2009_02