HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409774Generated: October 29, 2026
Trimethylsilyl iodide → HCID 57947570, compound
https://huagongshe.com/reaction/409774
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | HCID 57948010 | HCID 57948010 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 57947570 | HCID 57947570 | 60.1% |
Reaction Steps
To a solution of (S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-6-(dimethoxyphosphoryloxy)hexyl isoquinolin-3-ylcarbamate (0.28 g, 0.47 mmol, 1.0 equiv.) in acetonitrile (25 mL) was added TMSI (0.28 mL, 1.88 mmol, 4.0 equiv.) at RT After stirred at RT for 15 min, the reaction was quenched with MeOH. The solvent was concentrated. The resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H2O with 0.1% TFA. The fractions containing the product were combined and concentrated. The resulting residue was suspended in EtOAc, 5 drops of HCl (4 M in 1,4-dioxane) were added, and the organic solvent was removed. This procedure was repeated to give (S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-6-(phosphonooxy)hexyl isoquinolin-3-ylcarbamate (0.16 g, 57%) as a HCl salt. LRMS (M+H+) m/z 567.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08759374B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-3b9cd3e5eb244035bfa589fab494c5fe |
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| Source note | uspto-grants-2014_06 |
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