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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46194Generated: October 28, 2026

Sodium Methoxide → HCID 46228963, compound

https://huagongshe.com/reaction/46194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
Reactant(2S,3R,4R,5S,6S)-2-(acetoxymethyl)-6-(4-chloro-3-((5-(furan-2-yl)-1,3,4-thiadiazol-2-yl)methyl)phenyl)-tetrahydro-2H-pyran-3,4,5-triyl triacetateHCID 67287618—
ReactantHCID 178418361HCID 178418361—
SolventMethanolHCID 887—
ProductHCID 46228963HCID 4622896358.1%

Reaction Steps

To a solution of (2S,3R,4R,5S,6S)-2-(acetoxymethyl)-6-(4-chloro-3-((5-(furan-2-yl)-1,3,4-thiadiazol-2-yl)methyl)phenyl)-tetrahydro-2H-pyran-3,4,5-triyl triacetate (187 mg, 0.31 mmol) from Step 3 in methanol (10 mL) was added sodium methoxide (25 wt % in methanol, 1.0 mL). The reaction mixture was stirred at ambient temperature for 2 h. Amberlite® IR120 hydrogen form was then added to neutralize the reaction mixture. The resin was filtered off and the filtrate was concentrated in vacuo. Purification by reverse phase preparative HPLC (Gilson®, SunFire™ Prep, 5 to 50% acetonitrile in water gradient) provided the title compound (78 mg, 0.18 mmol, 58%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541380B2
Source datasetuspto-grants-2013_09
ORD IDord-10e748bdcade4cd696cad0c4bc1367a9
Source noteuspto-grants-2013_09