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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342689Generated: October 25, 2026

4-[1-Hydroxy-5-(2-methylthiopyrimidin-4-yl)-4-(3-trifluoromethylphenyl)-1H-imidazol-2-yl]piperidine-1-carboxylic acid benzyl ester → 4-[5-(2-Methylthiopyrimidin-4-yl)-4-(3-trifluoromethylphenyl)-1H-imidazol-2-yl]piperidine-1-carboxylic acid benzyl ester

https://huagongshe.com/reaction/342689

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[1-Hydroxy-5-(2-methylthiopyrimidin-4-yl)-4-(3-trifluoromethylphenyl)-1H-imidazol-2-yl]piperidine-1-carboxylic acid benzyl esterHCID 10769362—
Catalysttitanium(III) trichlorideHCID 10313229—
SolventMethanolHCID 887—
Product4-[5-(2-Methylthiopyrimidin-4-yl)-4-(3-trifluoromethylphenyl)-1H-imidazol-2-yl]piperidine-1-carboxylic acid benzyl esterHCID 1065036378.6%

Reaction Steps

To a stirring solution of 4-[1-hydroxy-5-(2-methylthiopyrimidin-4-yl)-4-(3-trifluoromethylphenyl)-1H-imidazol-2-yl]piperidine-1-carboxylic acid benzyl ester (9.5 g. crude, 0.0146 mole) in methanol (130 mL) at 20° C. was added titanium (III) chloride (25 mL, 0.029 mole, 15% wt in 20-30% HCl) dropwise over 10 minutes. The reaction was allowed to stir for 3 hours then quenched by pouring slowly into a mixture of 10% aqueous sodium bicarbonate (1.5 L) and ethyl acetate (600 mL). After stirring for 30 minutes the organic layer was removed and aqueous extract washed with ethyl acetate (2×200 mL). The organic extracts were combined, dried over anhydrous sodium sulfate, and concentrated to an oil. The oil was chromatographed on silica using 60% ethyl acetate/hexane to give 6.35 g of a yellow foam upon concentration of product containing fractions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05859041
Source datasetuspto-grants-1999_01
ORD IDord-a9cd2e6d3d54448e80bef2640fe82970
Source noteuspto-grants-1999_01