HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 1-ethyl-6-methoxy-2-[4-(5-methyl-1,1-dioxo-1lambda6-[1,2,5]thiadiazolidin-2-yl)-phenyl]-1H-indole-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 59426210 | HCID 59426210 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-ethyl-6-methoxy-2-[4-(5-methyl-1,1-dioxo-1lambda6-[1,2,5]thiadiazolidin-2-yl)-phenyl]-1H-indole-3-carbonitrile | HCID 59425957 | — |
Reaction Steps
To a solution of 2-[4-(1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-2-yl)phenyl]-1-ethyl-6-methoxy-1H-indole-3-carbonitrile (34 mg, 0.086 mmol) in anhydrous DMF (1.0 mL) is added potassium carbonate (25 mg, 0.18 mmol) and iodomethane (20.4 mg, 0.144 mmol). The mixture is stirred at room temperature for 2 h and then diluted with water (6.0 mL) to give a precipitate. The precipitate is filtered, washed with water and dried to give 1-ethyl-6-methoxy-2-[4-(5-methyl-1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-2-yl)-phenyl]-1H-indole-3-carbonitrile, compound 726, as a white solid (35 mg, 98% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07973069B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-a98217d95eeb47e6a51b22a94bb6dae2 |
| Source note | uspto-grants-2011_07 |