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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929734Generated: November 2, 2026

Sodium Carbonate → 2-(4-Methoxyphenyl)-N-(4-methylbenzyl)-N-(1-(3-(1,3-dihydro-2H-benzimidazol-2-one-1-yl)propyl)piperidine-4yl)acetamide

https://huagongshe.com/reaction/929734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-oneHCID 1810419—
Reactant2-(4-Methoxyphenyl)-N-(4-methylbenzyl)-N-(piperidin-4-yl)acetamideHCID 9946526—
SolventAcetonitrileHCID 6342—
Product2-(4-Methoxyphenyl)-N-(4-methylbenzyl)-N-(1-(3-(1,3-dihydro-2H-benzimidazol-2-one-1-yl)propyl)piperidine-4yl)acetamideHCID 10119088—

Reaction Conditions

Temperature82 °C

Reaction Steps

50ELH87 (0.05 g, 0.14 mmol, 1 eq.) was transferred to a 4 ml vial and dissolved in 1 ml of acetonitrile. Then, 1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one (0.032 g, 1.1 eq.), sodium carbonate (0.022 g, 1.1 eq.) and KI (one crystal) were added and the vial was sealed and shaken for 20 h at 82° C. The mixture was extracted with distilled water (pH 10, sodium carbonate) and dichloromethane (3 times) the organic layers were dried with sodium sulfate and concentrated. The title compound was purified by HPLC and evaporated to dryness, forming a trifluoroacetic acid salt. Yield 8.8 mg (12%). UV/MS 100/100 (M+ 527), rt (A, MS) 2.851.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296694B2
Source datasetuspto-grants-2016_03
ORD IDord-37be4347c69b421bbc90e6725ecd5205
Source noteuspto-grants-2016_03