HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 2-(3-iodo-1H-indol-5-yl)-5-(methylthio)-1,3,4-thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-(1H-indol-5-yl)-5-(methylthio)-1,3,4-thiadiazole | HCID 68328215 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(3-iodo-1H-indol-5-yl)-5-(methylthio)-1,3,4-thiadiazole | HCID 68328312 | 75.2% |
Reaction Steps
To a solution of 2-(1H-indol-5-yl)-5-(methylthio)-1,3,4-thiadiazole (18.5 g, 74.8 mmol) in DMF (190 mL) was added KOH (16.2 g, 299 mmol) followed by I2 (38 g, 149.7 mmol). The reaction was stirred at RT for 2 h, and was quenched with 10% aq sodium bisulphate solution. The resulting precipitate was filtered and washed with H2O to give 2-(3-iodo-1H-indol-5-yl)-5-(methylthio)-1,3,4-thiadiazole (21 g, 75%). MS (ESI, pos. ion) m/z: 373.8 (M+1). 1HNMR (DMSO-d6, 300 MHz): 2.8 (s, 3H), 7.5 (d, 1H), 7.7 (m, 2H), 12.0 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321756B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-8ebd26ce063e426a90eaf61199b0a3ee |
| Source note | uspto-grants-2016_04 |