HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium peroxymonosulphate → 6-chloro-2-(methylsulfonyl)-3H-imidazo[4,5-c]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium peroxymonosulphate | HCID 10313463 | — |
| Reactant | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Reactant | 6-Chloro-2-(methylthio)-3H-imidazo[4,5-c]pyridine | HCID 90042108 | — |
| Product | 6-chloro-2-(methylsulfonyl)-3H-imidazo[4,5-c]pyridine | HCID 90042073 | — |
Reaction Steps
To a stirring solution of 6-chloro-2-(methylthio)-3H-imidazo[4,5-c]pyridine (954.0 mg, 4.78 mmol) in 50% CH3CN/water (61.4 mL) was added potassium peroxymonosulfate (oxone, 6.46 g, 10.51 mmol). The reaction was stirred under N2 at RT for 15 h, then filtered and the filtrate added to a stirring mixture of EtOAc (1.27 L)/water (0.70 L). The aqueous layer was separated and back-extracted with EtOAc (0.25 L). The combined organic layers were evaporated under reduced pressure to afford the title compound. LC-MS: calculated for C7H6ClN3O2S 230.99 observed m/e: 231.98 (M+H)+ (Rt 1.72/2.0 min)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09290517B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-08fa05f92f9845bb87f9b0b0cc83139a |
| Source note | uspto-grants-2016_03 |