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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606570Generated: October 30, 2026

Trimethyl orthoacetate → Benzoic acid, 4-[2-[4-(2-methoxyethyl)-1-piperazinyl]-4-thiazolyl]-

https://huagongshe.com/reaction/606570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoacetateHCID 15050—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-[2-(Piperazin-1-yl)-1,3-thiazol-4-yl]benzoic acidHCID 67047480—
SolventHydrochloric AcidHCID 313—
SolventAcetonitrileHCID 6342—
SolventSodium AcetateHCID 517045—
ProductBenzoic acid, 4-[2-[4-(2-methoxyethyl)-1-piperazinyl]-4-thiazolyl]-HCID 1165314751.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

4-[4-(4-Carboxy-phenyl)-thiazol-2-yl]-piperazine-1-carboxylic acid tert-butyl ester (5.0 mmol) was dissolved in hydrochloric acid in dioxane (4N, 25 ml) and the reaction stirred at RT for 2 h. The reaction was concentrated in vacuo to yield 4-(2-piperazin-1-yl-thiazol-4-yl)-benzoic acid. Trimethoxyethane (6.5 mmol) was dissolved in aqueous hydrochloric acid (1N, 10 ml) and the reaction heated at 50° C. for 1.5 h. The reaction was allowed to cool to RT and was then added to a suspension of 4-(2-piperazin-1-yl-thiazol-4-yl)-benzoic acid (5.0 mmol) in acetonitrile (25 ml) and sodium acetate buffer (1N, pH 5.5, 10 ml). The reaction was stirred at RT for 1.5 h. Sodium cyanoborohydride (6.5 mol) was added and the reaction stirred at RT for 16 h. The reaction was concentrated in vacuo and the product purified by flash chromatography (silica gel, 10% methanol in dichloromethane) to give the title product as a colourless oil (0.9 g). m/z=348 (100% M+H) in MS ES+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915300B2
Source datasetuspto-grants-2011_03
ORD IDord-185e9e6e50c5478fb233f0c9c0c1b0dc
Source noteuspto-grants-2011_03