HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416416Generated: October 30, 2026
Trimethylsilyl iodide → HCID 57947564, compound
https://huagongshe.com/reaction/416416
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | HCID 57947350 | HCID 57947350 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 57947564 | HCID 57947564 | 71.1% |
Reaction Steps
To a solution of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(dimethoxyphosphoryloxy)-4,4-dimethylpentyl 6-fluoroisoquinolin-3-ylcarbamate (0.5 g, 0.79 mmol) in acetonitrile (50 mL) was added TMSI (0.848 mL, 6.23 mmol) at 0° C. After stirred at 0° C. for 30 min, the reaction was quenched with MeOH. The solvent was removed and the resulting residue was purified on RP-HPLC using a mixture of acetonitrile and water (0.1% HCOOH buffer) to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,4-dimethyl-5-(phosphonooxy)pentyl 6-fluoroisoquinolin-3-ylcarbamate (340 mg, 71.1%). LRMS (M+H+) m/z 615.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088793B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-ddd9ae3807b14fc4998ff2379dee9436 |
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| Source note | uspto-grants-2012_01 |
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