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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045934Generated: October 31, 2026

Sodium methanethiolate → 2-(methylthio)-N-(3-(quinoxalin-2-yl)phenyl)acetamide

https://huagongshe.com/reaction/2045934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
ReactantHCID 46916455HCID 46916455—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product2-(methylthio)-N-(3-(quinoxalin-2-yl)phenyl)acetamideHCID 4691645675%

Reaction Steps

A slurry of 2-bromo-N-(3-(quinoxalin-2-yl)phenyl)acetamide (207 mg, 0.605 mmol) and sodium thiomethoxide (127 mg, 1.82 mmol) in ethanol (10 mL) was stirred at room temperature for 18 hrs. The reaction mixture was diluted with water (10 mL) and ethyl acetate (50 mL), the organic phase was separated, dried over sodium sulphate and evaporated in vacuo to afford 2-(methylthio)-N-(3-(quinoxalin-2-yl)phenyl)acetamide (140 mg, 75% yield). LCMS calculated for C17H15N3OS (M+H): 310.39. found 310. 1H-NMR (DMSO-d6, 400 Mhz) δH: 10.30 (1H, br.), 9.53 (1H, s), 8.53 (1H, m), 8.12-8.18 (2H, m), 8.05-8.08 (1H, m), 7.84-7.95 (3H, m), 7.55-7.60 (1H, m), 3.35 (2H, s), 2.22 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592415B2
Source datasetuspto-grants-2013_11
ORD IDord-037c51fdced44adb9cd238ccc16812b1
Source noteuspto-grants-2013_11