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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781388Generated: November 1, 2026

Water → HCID 19045487, compound

https://huagongshe.com/reaction/1781388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 19045479HCID 19045479—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventMethanolHCID 887—
ProductHCID 19045487HCID 1904548744.6%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 6-methanesulfonamido-3,4-dihydro-1'-(2-methylthioethyl)spiro[(2H)-1-benzopyran-2,4'-piperidine]-4-one (0.335 g, 0.871 mmol) in 15 mL of methanol was treated dropwise with a solution of Oxone® (0.803 g, 1.31 mmol) in 15 mL of water. The resulting mixture was stirred at 25° C. for 2 hours. The reaction mixture was then poured into 50 mL of saturated aqueous NaHCO3 and extracted with a total of 100 mL of ethyl acetate. The organic phase was dried (MgSO4), filtered, and concentrated in vacuo to a pale yellow oil which was shown to be a mixture by then layer analysis. The mixture was chromatographed on silica gel using 5% methanol in methylene chloride eluant. The pure oil was dissolved in 20 mL of absolute ethanol and was treated with excess 4.8N ethanolic HCl. The solid was collected, washed with diethyl ether, and dried for 4 hours at 100° C. under vacuum to give 0.176 g (44.6%) of product, mp 250°-251° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05633247
Source datasetuspto-grants-1997_05
ORD IDord-21549f1abd034e7fa819e5d32eb716a4
Source noteuspto-grants-1997_05