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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357664Generated: October 31, 2026

Sodium Hydroxide → 4-[2-(4-Tert-butoxycarbonylpiperazin-1-yl)thiazol-4-ylmethoxy]benzoic acid

https://huagongshe.com/reaction/1357664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantTert-butyl 4-(4-(4-methoxycarbonylphenoxymethyl)thiazol-2-yl]piperazine-1-carboxylateHCID 18186636—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-[2-(4-Tert-butoxycarbonylpiperazin-1-yl)thiazol-4-ylmethoxy]benzoic acidHCID 18186513100.9%

Reaction Conditions

Temperature55 °C

Reaction Steps

A solution of tert-butyl 4-(4-(4-methoxycarbonylphenoxymethyl)thiazol-2-yl]piperazine-1-carboxylate (820 mg, 1.89 mmol) in methanol (30 mL) and THF (10 mL) was treated with a solution of sodium hydroxide (226 mg, 5.67 mmol) in water (10 mL). The mixture was stirred at 55 ° C. for 8 hours and then concentrated by evaporation. The aqueous solution was diluted with water (10 mL) and the dilution was acidified with dilute hydrochloric acid. A resulting solid was collected by filtration to provide 4-[2-(4-tert-butoxycarbonylpiperazin-1-yl)thiazol-4-ylmethoxy]benzoic acid (800 mg, 100% yield). HNMR (dmso-d6): 7.88 (2H, d), 7.09 (2H, d), 6.91 (1H, s), 4.99 (2H, s), 3.44 (8H, m), 1.41 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06593327B2
Source datasetuspto-grants-2003_07
ORD IDord-d4ad9272a4154453b389e3f0742eba1a
Source noteuspto-grants-2003_07