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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807274Generated: October 31, 2026

Lithium hydroxide, monohydrate → Rac 4-{[(2r,3s,4r,5s)-4-(4-chloro-2-fluoro-phenyl)-3-(3-chloro-2-fluoro-phenyl)-4-cyano-5-(2,2-dimethyl-propyl)-pyrrolidine-2-carbonyl]-amino}-2-ethoxy-benzoic acid

https://huagongshe.com/reaction/1807274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactantracemic methyl 4-((2R,3S,4R,5S)-3-(3-chloro-2-fluorophenyl)-4-(4-chloro-2-fluorophenyl)-4-cyano-5-neopentylpyrrolidine-2-carboxamido)-2-ethoxybenzoateHCID 67368577—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductRac 4-{[(2r,3s,4r,5s)-4-(4-chloro-2-fluoro-phenyl)-3-(3-chloro-2-fluoro-phenyl)-4-cyano-5-(2,2-dimethyl-propyl)-pyrrolidine-2-carbonyl]-amino}-2-ethoxy-benzoic acidHCID 53357879—

Reaction Conditions

Temperature70 °C

Reaction Steps

In a manner similar to the method described in Example 380, a solution of the above methyl 4-((2R,3S,4R,5S)-3-(3-chloro-2-fluorophenyl)-4-(4-chloro-2-fluorophenyl)-4-cyano-5-neopentylpyrrolidine-2-carboxamido)-2-ethoxybenzoate (89.7 mg, ˜0.13 mmol) in THF (8 ml) was treated with lithium hydroxide hydrate (40.9 mg, 0.974 mmol) in water (4 mL) and heated at 70° C. for 3 hrs and then stirred at room temperature to give rac 4-{[(2R,3S,4R,5S)-4-(4-Chloro-2-fluoro-phenyl)-3-(3-chloro-2-fluoro-phenyl)-4-cyano-5-(2,2-dimethyl-propyl)-pyrrolidine-2-carbonyl]-amino}-2-ethoxy-benzoic acid as a white lyophilized solid (33.5 mg., 38%) after HPLC purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354444B2
Source datasetuspto-grants-2013_01
ORD IDord-eb68b2815f3849048df2192ea6f8dd5d
Source noteuspto-grants-2013_01