HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Thiosulfate → HCID 15949406, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | HCID 15949401 | HCID 15949401 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 15949406 | HCID 15949406 | 78.4% |
Reaction Steps
A solution of 3-[(9-chloro-4-methyl-5-oxo-2,3,4,5-tetrahydro-1,4-benzoxazepin-8-yl)oxy]-N-(1-ethyl-1H-pyrazol-3-yl)-5-{[(1S)-1-methyl-2-(methyloxy)ethyl]oxy}benzamide (300 mg, 0.57 mmol) in acetonitrile (10 mL) was treated with trimethylsilyl iodide (0.404 mL) and stirred at RT under argon for 3 hours. Sodium thiosulphate solution (30 mL) was added to quench the reaction and mixture was extracted with ethyl acetate (3×30 mL). The combined organic extracts were dried (MgSO4), filtered and evaporated to give a yellow oil. Purification by column chromatography on silica, eluting with 50-100% ethyl acetate in hexanes, gave the desired compound as a pale yellow solid (230 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07943607B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-d5d012069b6141498258c260652ed24c |
| Source note | uspto-grants-2011_05 |