Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11667Generated: October 25, 2026

Lithium hydroxide, monohydrate → 5-Chloro-2-{2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-N-(2-hydroxy-2-methyl-propionyl)-benzenesulfonamide

https://huagongshe.com/reaction/11667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantAcetic Acid 2-(5-Chloro-2-{2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-benzenesulfonylamino)-1,1-dimethyl-2-oxo-ethyl EsterHCID 69655351—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-2-{2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-N-(2-hydroxy-2-methyl-propionyl)-benzenesulfonamideHCID 6965573789.1%

Reaction Steps

To a solution of acetic acid 2-(5-chloro-2-{2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-benzenesulfonylamino)-1,1-dimethyl-2-oxo-ethyl ester (0.14 g, 0.21 mmol) in tetrahydrofuran (2 mL), methanol (0.2 mL) and water (0.4 mL) was added lithium hydroxide monohydrate (0.020 g, 0.48 mmol). The resulting reaction mixture was stirred at ambient temperature overnight. Chromatography on silica gel of the reaction mixture provided the title compound (0.104 g, LRMS: 556.3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098212B2
Source datasetuspto-grants-2006_08
ORD IDord-8e14bb657fa8415fa72446efe618afdc
Source noteuspto-grants-2006_08