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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048575Generated: November 1, 2026

Acetic Acid → HCID 58573370, compound

https://huagongshe.com/reaction/1048575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantPotassium PermanganateHCID 516875—
ReactantHCID 68000252HCID 68000252—
CatalystTetrabutylammonium chloride hydrateHCID 16212273—
SolventDichloromethaneHCID 6344—
ProductHCID 58573370HCID 58573370—

Reaction Steps

A solution of (3S,5R,6S)-3-allyl-1-((S)-1-(tert-butylthio)butan-2-yl)-6-(4-chlorophenyl)-5-(5-chloropyridin-3-yl)-3-methylpiperidin-2-one (Example 401, Step A, 0.147 g, 0.283 mmol;) with acetic acid (0.972 mL, 16.98 mmol) and tetrabutylammonium chloride hydrate (8.37 mg, 0.028 mmol) in 4 ml of DCM was cooled in an ice bath. A solution of potassium permanganate (0.268 g, 1.698 mmol) in 3 mL of water was added. The purple solution was stirred while cooling with an ice bath and allowed to warm to room temperature over 2 hours. Aq. NaS2O3 solution was added along with additional DCM. After filtering the solution through filter paper the filtrate was partitioned and then the aq. layer was washed with DCM. The combined organics were dried over Na2SO4 and concentrated. The product was purified by silica gel chromatography followed by preparatory HPLC (Agilent column, EXTEND C18 PrepHT, 5 uM, 30×250 mm) eluting with a gradient of 20% MeCN/H2O/0.1% TFA to 80% MeCN/H2O/0.1% TFA over 25 minutes. The fractions containing the product were combined, frozen in a acetone/dry ice bath and the solvents were removed on a lyophilizer to provide the title compound as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569341B2
Source datasetuspto-grants-2013_10
ORD IDord-047b6fdedce94c22975c71b7496b5fb8
Source noteuspto-grants-2013_10