HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Thiosulfate → HCID 15949498, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | HCID 15949403 | HCID 15949403 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 15949498 | HCID 15949498 | 41.6% |
Reaction Steps
A solution of N-(1-ethyl-1H-pyrazol-3-yl)-3-{[(1S)-1-methyl-2-(methyloxy)ethyl]oxy}-5-[(4-methyl-5-oxo-2,3,4,5-tetrahydro-1,4-benzoxazepin-8-yl)oxy]benzamide (125 mg, 0.25 mmol) in acetonitrile (5 mL) was treated with trimethylsilyl iodide (0.178 mL) drop wise and stirred at RT under argon for 2.5 hours. Aqueous sodium thiosulphate solution (30 mL) was added to quench the reaction and the 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 was carried out by column chromatography on silica, eluting with 50-100% ethyl acetate in isohexane, to give the desired compound as a pale yellow foam (50 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07943607B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-c8c4d1e9fa0147fb80fe99e0b363766b |
| Source note | uspto-grants-2011_05 |