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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245881Generated: November 3, 2026

Hydrochloric Acid → HCID 58815887, compound

https://huagongshe.com/reaction/2245881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 12004032HCID 12004032—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58815887HCID 5881588766%

Reaction Steps

To a solution of 1-{3-[(R)-((2S,5R)-4-benzyl-2,5-dimethyl-piperazin-1-yl)-(3-hydroxy-phenyl)-methyl]-benzoyl}-piperidine-4-carboxylic acid ethyl ester (365 mg, Example 122) in THF (4 mL) was added 1N NaOH solution (3 mL). The reaction was stirred at room temperature overnight. The reaction solution was neutralized by the addition of 1 N HCl solution (3 mL). The resulting solution was concentrated under vacuum to give crude product, which was subjected to reverse phase C-18 column chromatography conducted on CombiFlash™ Sq 16×(gradient: 100% H2O to 100% MeOH) to give 1-{3-[(R)-((2S,5R)-4-benzyl-2,5-dimethyl-piperazin-1-yl)-(3-hydroxy-phenyl)-methyl]-benzoyl}-piperidine-4-carboxylic acid (228 mg; 66%). 1H NMR (300 MHz, CD3OD) δ 7.49 (m, 2H), 7.38 (m, 6H), 7.28 (m, 1H), 7.18 (dd, J=8.0, 8.0 Hz, 1H), 6.73 (m, 2H), 6.67 (s, 1H), 5.26 (s, 1H), 4.48 (m, 1H), 4.27 (d, J=13.0 Hz, 1H), 3.66 (m, 2H), 3.13 (m, 1H), 3.01 (m, 2H), 2.85 (m, 2H), 2.68 (m, 1H), 2.49 (m, 2H), 2.13 (dd, J=10.5, 10.5 Hz, 1H), 2.00 (m, 1H), 1.82 (m, 1H), 1.65 (m, 2H), 1.28 (d, J=6.5 Hz, 3H), 1.17 (d, J=6.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683168B2
Source datasetuspto-grants-2010_03
ORD IDord-4f3164079464412e9b336a137336cf33
Source noteuspto-grants-2010_03