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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909855Generated: October 29, 2026

1,3-Dimethyl-2-imidazolidinone → HCID 58306650, compound

https://huagongshe.com/reaction/1909855

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dimethyl-2-imidazolidinoneHCID 6661—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Bromomethyl)-4-chlorobenzeneHCID 69329—
ReactantHCID 58306597HCID 58306597—
SolventWaterHCID 962—
ProductHCID 58306650HCID 5830665027.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

To methyl 4-[(1S)-1-({[2-(methylamino)-4,5,6,7-tetrahydro-1-benzothien-3-yl]carbonyl}amino)ethyl]benzoate (0.41 g) was added 1,3-dimethyl-2-imidazolidinone (4.0 mL), and potassium carbonate (0.30 g) and 1-(bromomethyl)-4-chlorobenzene (0.34 g) were added thereto under ice-cooling, followed by stirring at 50° C. overnight. The reaction mixture was cooled to room temperature, and then water (50 mL) was added thereto, followed by extraction with ethyl acetate. The obtained organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate: 15/1-4/1) to obtain methyl 4-{(1S)-1-[({2-[(4-chlorobenzyl)(methyl)amino]-4,5,6,7-tetrahydro-1-benzothiophen-3-yl}carbonyl)amino]ethyl}benzoate (0.15 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598355B2
Source datasetuspto-grants-2013_12
ORD IDord-74a27b1fcd3a426cb357289770bbed90
Source noteuspto-grants-2013_12