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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269861Generated: October 31, 2026

Lithium hydroxide, monohydrate → 4-[2-(1-{2-[3-(3,4-Dichloro-phenyl)-1-(3,4,5-trimethoxy-benzoyl)-pyrrolidin-3-yl]-ethyl}-piperidine-4-carbonyl)-benzoimidazol-1-yl]-butyric acid

https://huagongshe.com/reaction/2269861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant4-[2-(1-{2-[3-(3,4-Dichloro-phenyl)-1-(3,4,5-trimethoxy-benzoyl)-pyrrolidin-3-yl]-ethyl}-piperidine-4-carbonyl)-benzoimidazol-1-yl]-butyric acid ethyl esterHCID 10147218—
ReactantOxolane--water (1/1)HCID 21881883—
SolventWaterHCID 962—
Product4-[2-(1-{2-[3-(3,4-Dichloro-phenyl)-1-(3,4,5-trimethoxy-benzoyl)-pyrrolidin-3-yl]-ethyl}-piperidine-4-carbonyl)-benzoimidazol-1-yl]-butyric acidHCID 10305888—

Reaction Conditions

Temperature5 °C

Reaction Steps

Combine 1-(3,4,5-trimethoxy-benzoyl)-3-[2-[4-[1-(3-ethoxycarbonyl-propyl)-1 H-benzoimidazole-2-carbonyl]-piperidin-1-yl]-ethyl]-3-(3,4-dichloro-phenyl)-pyrrolidine (0.32 g, 0.41 mmol) and lithium hydroxide hydrate (0.052 g, 1.23 mmol) in 4/1 tetrahydrofuran/water (20 mL). After 20 hours, dilute the reaction mixture with water and evaporate in vacuo to remove most of the tetrahydrofuran. Acidify to pH 2 using 1 M hydrochloric acid solution and cool to 5° C. to obtain a solid. Collect the solid by filtration. Suspend the solid in diethyl ether (150 mL) and stir. After 18 hours, collect the solid by filtration and dry to give the title compound: mp; 125-140° C. Elemental Analysis calculated for C39H44Cl2N4O7·HCl: C 59.43; H 5.75; N 7.11; Found: C 59.55; H 5.81; N 6.94.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329392B1
Source datasetuspto-grants-2001_12
ORD IDord-7ef37a75824240c1ab1a47cd965dd0d9
Source noteuspto-grants-2001_12