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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340982Generated: October 29, 2026

Trimethylsilyl iodide → HCID 57947564, compound

https://huagongshe.com/reaction/340982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 57947350HCID 57947350—
SolventAcetonitrileHCID 6342—
ProductHCID 57947564HCID 5794756471.1%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895582B2
Source datasetuspto-grants-2014_11
ORD IDord-0000388822814505aa81f17c12d29c4a
Source noteuspto-grants-2014_11