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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 609680Generated: October 30, 2026

Hydrochloric Acid → 2-(R)-{[4-(5-chloropyridin-2-yloxy)piperidine-1-sulfonyl]amino}-3-methylbutyric acid

https://huagongshe.com/reaction/609680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactantmethyl (R)-2-{[4-(5-chloropyridin-2-yloxy)piperidine-1-sulfonyl]amino}-3-methylbutyrateHCID 15896080—
SolventWaterHCID 962—
SolventMeOH tetrahydrofuranHCID 21899815—
Product2-(R)-{[4-(5-chloropyridin-2-yloxy)piperidine-1-sulfonyl]amino}-3-methylbutyric acidHCID 1872713566%

Reaction Conditions

Temperature45 °C

Reaction Steps

A solution of lithium hydroxide monohydrate (0.35 g, 8.3 mmol) in water (5 ml) was added to a solution of methyl (R)-2-{[4-(5-chloropyridin-2-yloxy)piperidine-1-sulfonyl]amino}-3-methylbutyrate (1.7 g, 4.2 mmol), [prepared as described in Example 2], in methanol/tetrahydrofuran (1:1, 25 ml) and the reaction mixture was warmed to 45° C. After stirring overnight, reaction mixture was adjusted to pH 6 using 1M HCl and the product was extracted into ethyl acetate. The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was chromatographed (SiO2, 2% methanol/methylene chloride) to give 2-(R)-{[4-(5-chloropyridin-2-yloxy)piperidine-1-sulfonyl]amino}-3-methylbutyric acid as a white gummy solid (66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998412
Source datasetuspto-grants-1999_12
ORD IDord-60b81a7b85564bd99109b0f8296bcdfa
Source noteuspto-grants-1999_12