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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323500Generated: October 26, 2026

Diethyl Ether → 1-(3,4,5-Trimethoxybenzyl)-3-(3-(4-(1h-benzimidazol-2-yl-amino)piperidin-1-yl)propyl)-3-(4-fluorophenylmethyl)-2-oxopyrrolidine methanesulfonic acid salt

https://huagongshe.com/reaction/323500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantMethanesulfonic AcidHCID 6395—
Reactant1-(3,4,5-trimethoxybenzyl)-3-(3-(4-(1H-benzimidazol-2-yl-amino)piperidin-1-yl)propyl)-3-(4-fluorophenylmethyl)-2-oxopyrrolidineHCID 9895457—
SolventEthyl AcetateHCID 8857—
Product1-(3,4,5-Trimethoxybenzyl)-3-(3-(4-(1h-benzimidazol-2-yl-amino)piperidin-1-yl)propyl)-3-(4-fluorophenylmethyl)-2-oxopyrrolidine methanesulfonic acid saltHCID 22009175—

Reaction Steps

Combine 1-(3,4,5-trimethoxybenzyl)-3-(3-(4-(1H-benzimidazol-2-yl-amino)piperidin-1-yl)propyl)-3-(4-fluorophenylmethyl)-2-oxopyrrolidine (0.37 g, 0.56 mmol) and methanesulfonic acid (0.17 g, 1.8 mmol) in ethyl acetate (10 mL). Heat to reflux. After 1 hour, cool to ambient temperature, add diethyl ether (75 mL). After 12 hours, evaporate the solvent to give a residue. Triturate the residue with diethyl ether (80 mL) to give a solid. Collect the solid and dry to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211199B1
Source datasetuspto-grants-2001_04
ORD IDord-84938087964e4fd7b8ba0437d9c481a7
Source noteuspto-grants-2001_04