HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 3-iodo-5-(6-isopropoxypyrazin-2-yl)-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-(6-propan-2-yloxypyrazin-2-yl)-1H-indole | HCID 67959718 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-iodo-5-(6-isopropoxypyrazin-2-yl)-1H-indole | HCID 67959958 | 102.6% |
Reaction Steps
To a solution of 5-(6-isopropoxy-pyrazin-2-yl)-1H-indole (32 g, 0.126 mol) in DMF (250 mL) was added KOH (17.8 g, 0.316 mol) and then stirred for 15 min at RT. I2 (35.3 g, 0.139 mol) was added to the reaction mixture and stirred at RT for another 1 h. Then reaction mixture was poured into ice water and excess of I2 was quenched with sodium thiosulfite. The resulting solid was collected by filtration, washed with water and dried under vacuum to afford crude 3-iodo-5-(6-isopropoxypyrazin-2-yl)-1H-indole (49 g) as pale brown solid. MS (ESI, m/z): 379.9 (M+1). This material was used to further step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09090593B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-548cb172099348ad950af735bdcd369c |
| Source note | uspto-grants-2015_07 |