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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507495Generated: October 31, 2026

Sodium Iodide → (R)-5-(2-(1H-pyrrol-1-yl)thiazol-4-yl)-2-morpholino-6-(piperidin-3-ylamino)pyrimidin-4(3H)-one

https://huagongshe.com/reaction/1507495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant(R)-tert-butyl 3-((5-(2-(1H-pyrrol-1-yl)thiazol-4-yl)-6-methoxy-2-morpholinopyrimidin-4-yl)amino)piperidine-1-carboxylateHCID 117677378—
SolventAcetonitrileHCID 6342—
Product(R)-5-(2-(1H-pyrrol-1-yl)thiazol-4-yl)-2-morpholino-6-(piperidin-3-ylamino)pyrimidin-4(3H)-oneHCID 136272323—

Reaction Steps

To (R)-tert-butyl 3-((5-(2-(1H-pyrrol-1-yl)thiazol-4-yl)-6-methoxy-2-morpholinopyrimidin-4-yl)amino)piperidine-1-carboxylate (xx) (0.08 g, 0.148 mmol) in MeCN (2.95 ml) was added NaI (0.033 g, 0.222 mmol) followed by TMS-Cl (0.028 ml, 0.222 mmol) under argon. The reaction was stirred at room temperature for 15 min., then heated to 50° C. for 2 h until the reaction was complete, monitored by LCMS. The solvent was removed and the reaction material was purified by preparative HPLC to give the title compound. MS (m/z)=428 (M+H). IRAK4 IC50=12 nM

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221809B2
Source datasetuspto-grants-2015_12
ORD IDord-0f3513904d9349af90b1d52dcf51b6a3
Source noteuspto-grants-2015_12