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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333415Generated: October 30, 2026

Iodoethane → 6-ethyl-7,8-dihydroimidazo[1,5-c]pyrimidin-5(6H)-one

https://huagongshe.com/reaction/333415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
Reactant5H,6H,7H,8H-imidazo(1,5-c)pyrimidin-5-oneHCID 1487518—
SolventDimethylformamideHCID 6228—
Product6-ethyl-7,8-dihydroimidazo[1,5-c]pyrimidin-5(6H)-oneHCID 12647284—

Reaction Steps

To 500 mg (3.6 mmol) of 5,6,7,8-tetrahydro-5-oxoimidazo[1,5-c]pyrimidine dissolved in 5 mL of DMF are added cautiously at room temperature 173 mg (4.32 mmol) of sodium hydride. The reaction medium is stirred for 1 hour at room temperature, and 0.35 mL (4.32 mmol) of iodoethane is then added dropwise. The reaction medium is stirred for 2 hours at room temperature and the solvents are then evaporated off. The residue is treated with 1N NaHCO3 solution and extracted with chloroform. The combined organic phases are dried with MgSO4, filtered and evaporated. The oil obtained is used directly in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877968B2
Source datasetuspto-grants-2014_11
ORD IDord-b9fc3996d22b4207a971a1dc312ba64b
Source noteuspto-grants-2014_11