HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Thiosulfate → 6-chloro-3-methyl-4-(methylsulfonyl)-3H-imidazo[4,5-c]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 6-chloro-3-methyl-4-(methylthio)-3H-imidazo[4,5-c]pyridine | HCID 117843414 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-chloro-3-methyl-4-(methylsulfonyl)-3H-imidazo[4,5-c]pyridine | HCID 117842888 | — |
Reaction Steps
To a solution of 6-chloro-3-methyl-4-(methylthio)-3H-imidazo[4,5-c]pyridine 2.02 (450 mg, 2.11 mmol) in dichloromethane (16 mL) at 0° C., was added mCPBA (≦77%, 972 mg, 4.34 mmol) and mixture was warmed to room temperature. After 80 minutes, an additional 200 mg of mCPBA was added. After an additional twenty minutes, a solution of 50% saturated Na2S2O3 (aq) (20 mL) was added and reaction mixture stirred at room temperature for fifteen minutes. Layers were separated and aqueous was extracted with ethyl acetate (4×15 mL). All organic layers were combined, washed with saturated NaHCO3 (aq) (2×30 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure to yield 6-chloro-3-methyl-4-(methylsulfonyl)-3H-imidazo[4,5-c]pyridine 2.04.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09376441B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-805407c88c194a49bb78907c01418752 |
| Source note | uspto-grants-2016_06 |