HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → HCID 59238645, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 59238626 | HCID 59238626 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59238645 | HCID 59238645 | — |
Reaction Steps
To a stirred solution of the azaindole (XIb-19) (2.51 g, 9.72 mmol) in DMF (40 mL), was added crushed KOH pellets (2.05 g, 36.6 mmol) followed by I2 (2.22 g, 8.7 mmol). The mixture was stirred at room temperature for 3.5 h and concentrated in vacuum. The residue was partitioned between EtOAc (100 mL) and saturated aqueous NaHCO3 solution (40 mL). The aqueous layer was extracted with EtOAc (3×60 mL). The combined organic solutions were dried (MgSO4), filtered and concentrated. The residue consisting of crude iodide (XIIb-19) was used for the preparation of (IXb-19) without any additional purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08178552B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-bcaf6062aaf14e828f286fee589fa231 |
| Source note | uspto-grants-2012_05 |