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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245103Generated: October 30, 2026

(2R)-3-Chloro-1,2-propanediol → (R)-3-{4-[5-(2-Cyclopentyl-6-methoxy-pyridin-4-yl)-[1,2,4]oxadiazol-3-yl]-2-ethyl-6-methyl-phenoxy}-propane-1,2-diol

https://huagongshe.com/reaction/245103

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2R)-3-Chloro-1,2-propanediolHCID 148793—
Reactant4-[5-(2-Cyclopentyl-6-methoxy-pyridin-4-yl)-[1,2,4]oxadiazol-3-yl]-2-ethyl-6-methyl-phenolHCID 136391015—
SolventIsopropanolHCID 3776—
SolventEthyl AcetateHCID 8857—
SolventSodium HydroxideHCID 14798—
Product(R)-3-{4-[5-(2-Cyclopentyl-6-methoxy-pyridin-4-yl)-[1,2,4]oxadiazol-3-yl]-2-ethyl-6-methyl-phenoxy}-propane-1,2-diolHCID 4987197499.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 4-[5-(2-cyclopentyl-6-methoxy-pyridin-4-yl)-[1,2,4]oxadiazol-3-yl]-2-ethyl-6-methyl-phenol (250 mg, 659 μmol), (R)-3-chloro-1,2-propanediol (609 mg, 6.59 mmol) in isopropanol (8 mL) and 3 M aq. NaOH (2 mL) is stirred at 60° C. for 15 h. The mixture is diluted with EA and washed with brine, 1 M aq. NaOH and again with brine. The org. extract is dried over Na2SO4, filtered and concentrated. The crude product is purified on prep. TLC plates using DCM containing 10% of methanol to give the title compound (297 mg) as a pale yellow oil; LC-MS**: tR=0.87 min, [M+H]+=454.26.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658675B2
Source datasetuspto-grants-2014_02
ORD IDord-36456c5c4b79498eae343c8109ca9824
Source noteuspto-grants-2014_02