HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium methanethiolate → 2-(methylthio)-N-(3-(quinoxalin-2-yl)phenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | HCID 46916455 | HCID 46916455 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(methylthio)-N-(3-(quinoxalin-2-yl)phenyl)acetamide | HCID 46916456 | 75% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08592415B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-037c51fdced44adb9cd238ccc16812b1 |
| Source note | uspto-grants-2013_11 |