HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 3-Iodo-5-phenylsulfanyl-1H-pyrrolo[2,3-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | 5-Phenylsulfanyl-1H-pyrrolo[2,3-b]pyridine | HCID 59128709 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Iodo-5-phenylsulfanyl-1H-pyrrolo[2,3-b]pyridine | HCID 59128705 | 98% |
Reaction Steps
To a solution of 2 (135 mg, 0.60 mmol) in DMF (1.5 mL) was added solid KOH (124 mg, 2.21 mmol) and the reaction mixture stirred for 20 min. Iodine (167 mg, 0.66 mmol) was then added and the stirring continued for 40 min. A mixture of water (8.8 mL) and sat. aq. Na2S2O3 (1.3 mL) was added rapidly, and the resulting solid filtered off, washed with water (2×) and dried in vacuum to give iodide 3 as a creamy solid (205 mg, 98%); 1H NMR (400 MHz, CDCl3+2 drops CD3OD) δ 7.10-7.30 (m, 5H), 7.45 (s, 1H), 7.94 (d, J=2.0 Hz, 1H), 8.35 (d, J=1.9 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07645769B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-333e844165204f2bb43227c41999f2f3 |
| Source note | uspto-grants-2010_01 |