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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504880Generated: November 2, 2026

Ethanol → HCID 68464556, compound

https://huagongshe.com/reaction/504880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium SulfiteHCID 24437—
ReactantPotassium hydroxy sulfiteHCID 23707502—
ReactantHCID 67487327HCID 67487327—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68464556HCID 6846455654%

Reaction Steps

To a mixture of N-methyl-N-{5-[3-(methylsulfonyl)propoxy]-2-[5-(thiomorpholinomethyl)-4,5-dihydro-1,3-thiazol-2-yl]-1H-indol-7-yl}pyridine-2-sulfonamide (0.35 g), ethanol (60 mL), water (30 mL) and tetrahydrofuran (30 mL) was added OXONE (registered trade mark, 0.19 g), and the mixture was stirred at room temperature for 3 hr. Aqueous sodium sulfite solution was added to the reaction mixture, the mixture was stirred for 30 min, and the organic solvent was evaporated under reduced pressure. The residue was diluted with water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained colorless crystals were recrystallized from ethyl acetate-hexane to give the title compound (193 mg, yield: 54%) as colorless crystals. MS: 641 (MH+). melting point 107-110° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07777047B2
Source datasetuspto-grants-2010_08
ORD IDord-49e2eec52ceb41fa855d490f81714b99
Source noteuspto-grants-2010_08