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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948531Generated: November 1, 2026

Isopropanol → 1-(2-Hydroxy-2-(4-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)-3-methylpiperidine-3-carboxylic acid

https://huagongshe.com/reaction/1948531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantCesium carbonateHCID 10796—
Reactant3-(4-(Oxiran-2-yl)phenyl)-5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazoleHCID 86656398—
SolventDimethyl SulfoxideHCID 679—
Product1-(2-Hydroxy-2-(4-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)-3-methylpiperidine-3-carboxylic acidHCID 50923841—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of ethyl 3-methylpiperidine-3-carboxylate, HCl (62.4 mg, 0.301 mmol), and cesium carbonate (98 mg, 0.301 mmol) in 2-propanol (2 mL) and DMSO (1 mL) was added 3-(4-(oxiran-2-yl)phenyl)-5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazole, Preparation 28C (30 mg, 0.075 mmol). The reaction mixture was heated at 80° C. overnight. The reaction mixture was filtered and purified by HPLC. HPLC conditions: PHENOMENEX® Luna 5 micron C18 column (30×100 mm); 10% MeOH/water (0.1% TFA)/90% MeOH/water (0.1% TFA); 10%-100% gradient over 15 minutes; 20 mL/min. Fraction with the correct mass were isolated and concentrated in vacuo. The residue was treated with 6N HCl/MeCN for 3 days and purified by HPLC. HPLC conditions: PHENOMENEX® Luna C18 5 micron column (250×30 mm); 25-100% CH3CN/water (0.1% TFA); 25 minute gradient; 30 mL/min. Isolated fractions with correct mass were freeze-dried overnight to yield 1 mg of 1-(2-hydroxy-2-(4-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethyl)-3-methylpiperidine-3-carboxylic acid as a TFA salt. MS (m+1)=543. HPLC Peak RT=3.29 minutes (Analytical Method A). Purity=95%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399451B2
Source datasetuspto-grants-2013_03
ORD IDord-cf4316f73ab1466fb6d51902091690a6
Source noteuspto-grants-2013_03