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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278586Generated: October 30, 2026

Potassium Iodide → 2-[1-(4-fluoro-2,3-dihydro-1H-indol-1-yl)-1-oxopropan-2-yl]-6-(morpholin-4-yl)pyrimidin-4(3H)-one

https://huagongshe.com/reaction/2278586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantAcetonitrileHCID 6342—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant1-(4-Fluoro-2,3-dihydroindol-1-yl)-2-(4-methoxy-6-morpholin-4-ylpyrimidin-2-yl)propan-1-oneHCID 68281581—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product2-[1-(4-fluoro-2,3-dihydro-1H-indol-1-yl)-1-oxopropan-2-yl]-6-(morpholin-4-yl)pyrimidin-4(3H)-oneHCID 13637868880.5%

Reaction Steps

210 mg of 1-(4-fluoro-2,3-dihydroindol-1-yl)-2-(4-methoxy-6-morpholin-4-yl-pyrimidin-2-yl)propan-1-one, 270 mg of potassium iodide, 7 ml of acetonitrile and 208 ml of trimethylchlorosilane are added to a microwave tube. After microwave irradiation for one hour at a temperature of 100° C., the reaction medium is diluted with 20 ml of ethyl acetate and 20 ml of water. After settling out, the organic phase is dried over magnesium sulfate, filtered, and then concentrated under reduced pressure. The residue obtained is stirred in the presence of 5 ml of ethyl acetate and 20 ml of petroleum ether. The solid obtained is filtered off and then dried under reduced pressure. 163 mg of 2-[1-(4-fluoro-2,3-dihydro-1H-indol-1-yl)-1-oxopropan-2-yl]-6-(morpholin-4-yl)pyrimidin-4(3H)-one are thus obtained in the form of a pale yellow solid, the characteristics of which are the following:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133168B2
Source datasetuspto-grants-2015_09
ORD IDord-fbe5718c43fa46b89d833049c0b41425
Source noteuspto-grants-2015_09