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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416400Generated: October 31, 2026

Trimethylsilyl iodide → HCID 57947533, compound

https://huagongshe.com/reaction/416400

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 57947544HCID 57947544—
SolventAcetonitrileHCID 6342—
ProductHCID 57947533HCID 5794753352%

Reaction Steps

(S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-5-(dimethoxyphosphoryloxy)pentyl isoquinolin-3-ylcarbamate (531 mg, 0.91 mmol) in acetonitrile (18 mL) was added TMSI (0.50 mL, 3.66 mmol) at 0° C. After stirred at RT for 10 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 H2O (0.1% HCOOH buffer) to give (S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-5-(phosphonooxy)pentyl isoquinolin-3-ylcarbamate (261 mg, 52%). LRMS (M+H+) m/z 553.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088793B2
Source datasetuspto-grants-2012_01
ORD IDord-4a672b9320df456998ef58672f4b6819
Source noteuspto-grants-2012_01