HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 619435Generated: November 1, 2026
Trimethylsilyl iodide → HCID 21190089, compound
https://huagongshe.com/reaction/619435
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 21190286 | HCID 21190286 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 21190089 | HCID 21190089 | 53.2% |
Reaction Steps
To a solution of 1.73 g (2.71 mmol) of 2-ethyl-3-trichloroacetyl-5-[N-tert-butoxycarbonyl-N-[5-(trifluoromethanesulfonamido)pentan-1-yl]aminomethyl]imidazo[1,2-a]pyridine in 15 ml of chloroform was added dropwise 0.80 ml (5.42 mmol) of iodotrimethylsilane at room temperature. The reaction mixture was stirred for 10 minutes, which was poured into ice-water, followed by neutralization with a saturated aqueous solution of sodium hydrogencarbonate. This solution was extracted with 100 ml of ethyl acetate. The organic layer was washed with 50 ml of 1.0N aqueous solution of sodium thiosulfate, then with 50 ml of a saturated aqueous saline solution. The organic layer was dried over magnesium sulfate, then the solvent was distilled off under reduced pressure. The residue was purified by silicagel column chromatography (eluent: chloroform/methanol=20:1) to give 603 mg of the desired compound (52.3%, pale yellow solid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05958942 |
|---|
| Source dataset | uspto-grants-1999_09 |
|---|
| ORD ID | ord-05bad01cb3a1489ba8e66623721f1f24 |
|---|
| Source note | uspto-grants-1999_09 |
|---|