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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323191Generated: October 29, 2026

Methanesulfonic Acid → 1-(3,4,5-Trimethoxybenzoyl)-3-(2-(4-(1-(2-ethoxyethyl)-1h-benzimidazol-2-yl-amino)piperidin-1-yl)ethyl)-3-(3,4-dimethoxyphenyl)pyrrolidine methanesulfonic acid salt

https://huagongshe.com/reaction/323191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantEthyl AcetateHCID 8857—
Reactant1-(3,4,5-trimethoxybenzoyl)-3-(2-(4-(1-(2-ethoxyethyl)-1H-benzimidazol-2-yl-amino)piperidin-1-yl)ethyl)-3-(3,4-dimethoxyphenyl)pyrrolidineHCID 9896590—
SolventDiethyl EtherHCID 3283—
Product1-(3,4,5-Trimethoxybenzoyl)-3-(2-(4-(1-(2-ethoxyethyl)-1h-benzimidazol-2-yl-amino)piperidin-1-yl)ethyl)-3-(3,4-dimethoxyphenyl)pyrrolidine methanesulfonic acid saltHCID 22009485—

Reaction Steps

Combine 1-(3,4,5-trimethoxybenzoyl)-3-(2-(4-(1-(2-ethoxyethyl)-1H-benzimidazol-2-yl-amino)piperidin-1-yl)ethyl)-3-(3,4-dimethoxyphenyl)pyrrolidine (0.48 g, 0.67 mmol) and ethyl acetate. Add a solution of methanesulfonic acid (2.2 mL, 0.77 M in ethyl acetate, 1.7 mmol). After 24 hours, add diethyl ether (150 mL) to form a solid. Decant solvent, add diethyl ether (200 mL) and stir. After 5 hours, decant solvent, add diethyl ether (200 mL). After 24 hours, collect the solid by filtration and dry in vacuo to give the title compound: mp; 125-130° C. Elemental Analysis calculated for C40H53N5O7 . 2 CH3SO3H . 2.43 H2O: C 53.00; H 6.97; N 7.36; Found: C 53.38; H 6.65; N 7.39.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211199B1
Source datasetuspto-grants-2001_04
ORD IDord-1f57dcb5350045a2bd049ebd54a608ee
Source noteuspto-grants-2001_04