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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593994Generated: November 1, 2026

Trimethylsilyl iodide → HCID 24856097, compound

https://huagongshe.com/reaction/593994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantAcetonitrile methylene chlorideHCID 21877088—
ReactantHCID 66731808HCID 66731808—
SolventMethanolHCID 887—
ProductHCID 24856097HCID 24856097—

Reaction Steps

To a slightly cloudy mixture of dibenzyl 4-(2-(4-(4-(4-methylthiazol-2-yl)phthalazin-1-ylamino)phenoxy)pyridin-3-yl)pyrimidin-2-ylphosphoramidate (0.086 g, 0.11 mmol) in 3 mL 5:1 ACN/DCM was added iodotrimethylsilane (0.16 ml, 1.1 mmol) dropwise via syringe at ambient temperature under nitrogen. After 5 min, 0.6 mL MeOH was added and the stir bar was removed. The reaction was concentrated in vacuo and suspended in DCM and filtered. The resulting orange solid was collected and dried in vacuo to provide 4-(2-(4-(4-(4-methylthiazol-2-yl)phthalazin-1-ylamino)phenoxy)pyridin-3-yl)pyrimidin-2-ylphosphoramidic acid dihydroiodide as an orange solid. MS m/z=585 [M+H]+. Calculated for C27H21N8O4PS: 584.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242961B2
Source datasetuspto-grants-2016_01
ORD IDord-e17d3d5b271349f39232d5cdd7a5dc33
Source noteuspto-grants-2016_01