HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinimide → 3-iodo-2-methyl-1H-pyrrolo[2,3-c]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 2-Methyl-1H-pyrrolo(2,3-c)pyridine | HCID 12407505 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-iodo-2-methyl-1H-pyrrolo[2,3-c]pyridine | HCID 67418512 | 92% |
Reaction Steps
2-Methyl-1H-pyrrolo[2,3-c]pyridine (100 mg, 0.76 mmol) was dissolved in CHCl3 (5 mL), N-iodosuccinimide (179 mg, 0.79 mmol) was added and the reaction mixture was stirred for 2 h. The reaction mixture was quenched with 1 M aq sodium thiosulphate (5 mL) and the CHCl3 was removed in vacuo. The reaction mixture was partitioned between sat aq NaHCO3 (40 mL) and EtOAc (40 mL). The aqueous layer was extracted with EtOAc (40 mL) and the combined organic fractions were washed with sat aq NaHCO3 (50 mL) and brine (50 mL), dried (MgSO4) and concentrated in vacuo to give the title compound as a cream solid (179 mg, 92%). LCMS (ES+): 258.9 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09227967B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-0bc03b6cdbca44099e42bb0342e9bb07 |
| Source note | uspto-grants-2016_01 |