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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416476Generated: November 2, 2026

Methyl iodide → HCID 67582994, compound

https://huagongshe.com/reaction/1416476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 67582038HCID 67582038—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 67582994HCID 6758299491.8%

Reaction Steps

To a solution of 2-[4-(benzyloxycarbonyl)piperazin-1-yl]-4-[(1S,4R)-(4-hydroxycyclopent-2-en-1-yl)oxy]quinazoline [cf. Example 33(3)] (750 mg) and methyl iodide (445 mg) in dimethylformamide (6 ml) is added 60% sodium hydride (oil) (94 mg) with stirring at room temperature, and the mixture is stirred at room temperature for 3 hours. The reaction mixture is diluted with ethyl acetate, and washed with water 5 times. The ethyl acetate solution is dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure. The resulting residue is purified by medium pressure liquid column chromatography [eluent, chloroform, (chloroform:methanol=200:1, v/v)] to give 2-[4-(benzyloxycarbonyl)piperazin-1-yl]-4-[(1S,4R)-(4-methoxycyclopent-2-en-1-yl)oxy]quinazoline (710 mg) as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05912247
Source datasetuspto-grants-1999_06
ORD IDord-ea46b6e6195944749dc7ad6c5acf637c
Source noteuspto-grants-1999_06