HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 2-(Methylthio)thiazolo[4,5-c]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 178527812 | HCID 178527812 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(Methylthio)thiazolo[4,5-c]quinoline | HCID 22648312 | — |
Reaction Steps
Sodium methoxide (15.8 mL of 25% in methanol, 69 mmol) and methyl iodide (3.9 mL, 63 mmol) were added to a solution of thiazolo[4,5-c]quinoline-2-thiol (13.65 g, 63 mmol) in methanol (160 mL). The reaction mixture was heated on a steam bath for 1 hour. The solvent was removed under vacuum. The resulting light green-yellow solid was slurried with water, isolated by filtration, and washed with water to provide 9.8 g of crude product. A portion (1 g) was recrystallized from methanol to provide 2-(methylthio)thiazolo[4,5-c]quinoline as a solid, m.p. 116–119° C. Analysis: Calculated for C11H8N2S2: % C, 56.87; % H, 3.47; % N, 12.06; Found: % C, 57.09; % H, 3.57; % N, 12.04.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07148232B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-ced5187b0b964054adeccae0c4440c63 |
| Source note | uspto-grants-2006_12 |