HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 619484Generated: October 30, 2026
Trimethylsilyl iodide → HCID 21190141, compound
https://huagongshe.com/reaction/619484
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 21190174 | HCID 21190174 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 21190141 | HCID 21190141 | 62.6% |
Reaction Steps
To a solution of 233 mg (0.50 mmol) of 3-hydroxymethyl-5-[N-tert-butoxycarbonyl-N-(3-trifluoromethanesulfonamidopropan-1-yl)aminomethyl]imidazo[1,2-a]pyridine in 5.0 ml of chloroform was added 0.36 ml (2.50 mmol) of trimethylsilyl iodide. The mixture was stirred for 18 hours at room temperature. The reaction mixture was poured into ice-water, which was neutralized with a saturated aqueous solution of sodium hydrogencarbonate, and extracted of the desired compound with 50 ml of chloroform. The organic layer was washed with 50 ml of a saturated aqueous saline solution and dried over magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (eluent; chloroform:methanol=20:1) to afford 109 mg of the desired compound (62.8%, a pale yellow liquid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05958942 |
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| Source dataset | uspto-grants-1999_09 |
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| ORD ID | ord-8d160fd72afe4d10b9f56d821a4e0d96 |
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| Source note | uspto-grants-1999_09 |
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