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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045937Generated: October 30, 2026

Potassium ethanethioate → HCID 46916461, compound

https://huagongshe.com/reaction/2045937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium ethanethioateHCID 23670855—
ReactantHCID 46916455HCID 46916455—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 46916461HCID 4691646113.5%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 2-bromo-N-(3-(quinoxalin-2-yl)phenyl)acetamide (300 mg, 0.876 mmol) and potassium thioacetate (400 mg, 3.5 mmol) in acetonitrile (15 mL) was heated in microwave at 140° C. for 10 min. The dark red solution was diluted with ethylacetate (50 mL), washed with brine (2×50 mL), dried over sodium sulphate, the solvent was evaporated in vacuo and the residue was purified by flash column chromatography (Flash Master, 20 g Isolute Silica column, gradient 0 to 5 min hexane, then ethyl acetate up to 50% over 20 min) to afford S-2-oxo-2-(3-(quinoxalin-2-yl)phenylamino)ethyl ethanethioate (40 mg, 13% yield). LCMS calculated for C18H15N3O2S (M+H): 338.40. found 338. 1H-NMR (DMSO-d6, 400 Mhz) δH: 10.45 (1H, br.), 9.50 (1H, s), 8.51 (1H, m), 8.11-8.18 (2H, m), 8.05-8.08 (1H, m), 7.80-7.95 (3H, m), 7.55-7.60 (1H, m), 3.90 (2H, s), 2.41 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592415B2
Source datasetuspto-grants-2013_11
ORD IDord-96913f5f374d4a8d8480c5906a5a9134
Source noteuspto-grants-2013_11