HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilyl iodide → HCID 178481616, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | HCID 178496592 | HCID 178496592 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178481616 | HCID 178481616 | — |
Reaction Steps
To an oven dried flask under Argon flow was added 3-(6-chloro-9-(trans-4-methoxycyclohexyl)-7-methyl-8-oxo-8,9-dihydro-7H-purin-2-yl)-3H-benzo[d]imidazole-5-carbonitrile (0.55 g, 1.25 mmol) in chloroform, followed by iodotrimethylsilane (0.1 mL, 1.25 mmol, 1 equiv.) The reaction mixture was stirred at room temperature for 4 h. Upon completion (HPLC monitoring), the reaction was slowly quenched with water. The organic layer was separated and the aqueous layer extracted with CHCl3 (15 ml×3) and with EtOAc (15 mL×3). The combined organic layers were dried (MgSO4), and concentrated in vacuo to give a dark solid (66% crude yield). MS (EI) m/z 424 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07902187B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-2a897d4e3dd24e6e8402315ec7c974d1 |
| Source note | uspto-grants-2011_03 |