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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942742Generated: November 4, 2026

Sodium Hydroxide → 1-{[3-(2-{3-Chloro-4-[(1-methylethyl)oxy]phenyl}-1,3-thiazol-5-yl)-2-ethylphenyl]methyl}-4-piperidinecarboxylic acid

https://huagongshe.com/reaction/1942742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 1-{[3-(2-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,3-thiazol-5-yl)-2-ethylphenyl]methyl}-4-piperidinecarboxylateHCID 58494151—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
Product1-{[3-(2-{3-Chloro-4-[(1-methylethyl)oxy]phenyl}-1,3-thiazol-5-yl)-2-ethylphenyl]methyl}-4-piperidinecarboxylic acidHCID 5457693948.2%

Reaction Steps

To a solution of ethyl 1-{[3-(2-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,3-thiazol-5-yl)-2-ethylphenyl]methyl}-4-piperidinecarboxylate (D85) (160 mg) in isopropanol (40 mL) and water (10 mL) stirred under nitrogen at room temperature was added a solution of NaOH (24.3 mg) in water in one charge. The reaction mixture was stirred at room temperature overnight. Isopropanol was removed in vacuo. The residue was dissolved in water and acidified with 1N HCl to pH=5. The solvent was removed in vacuo, the residue was dissolved in THF, and filtered. The filtrate was purified by Mass Directed AutoPrep to give 1-{[3-(2-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,3-thiazol-5-yl)-2-ethylphenyl]methyl}-4-piperidinecarboxylic acid (E36) (73 mg) as a TFA salt (white solid). δH (DMSO-d6, 400 MHz): 1.02 (3H, t), 1.34 (6H, d), 1.78 (2H, m), 2.05 (2H, m), 2.54 (1H, m), 2.83 (2H, m), 3.18 (2H, m), 3.45 (2H, m), 4.42 (2H, m), 4.80 (1H, m), 7.32 (1H, d), 7.44 (2H, m), 7.63 (1H, d), 7.87 (2H, m), 7.99 (1H, d), 9.28 (1H, br s), 12.59 (1H, br s). δF (DMSO-d6, 376 MHz): −74.0. MS (ES): C27H31ClN2O3S requires 498. found 499.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389508B2
Source datasetuspto-grants-2013_03
ORD IDord-1d3457d368f4447793e003121d4faf4a
Source noteuspto-grants-2013_03