HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilyl iodide → HCID 24856097, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | Acetonitrile methylene chloride | HCID 21877088 | — |
| Reactant | HCID 66731808 | HCID 66731808 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 24856097 | HCID 24856097 | — |
Reaction Steps
To a slightly cloudy mixture of dibenzyl 4-(2-(4-(4-(4-methylthiazol-2-yl)phthalazin-1-ylamino)phenoxy)pyridin-3-yl)pyrimidin-2-ylphosphoramidate (0.086 g, 0.11 mmol) in 3 mL 5:1 ACN/DCM was added iodotrimethylsilane (0.16 ml, 1.1 mmol) dropwise via syringe at ambient temperature under nitrogen. After 5 min, 0.6 mL MeOH was added and the stir bar was removed. The reaction was concentrated in vacuo and suspended in DCM and filtered. The resulting orange solid was collected and dried in vacuo to provide
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08686155B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-20329a34013841c3bddf7389567d5dbc |
| Source note | uspto-grants-2014_04 |