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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399769Generated: November 4, 2026

Benzyl Bromide → HCID 66955952, compound

https://huagongshe.com/reaction/1399769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 136346168HCID 136346168—
SolventDimethylformamideHCID 6228—
ProductHCID 66955952HCID 66955952—

Reaction Steps

LHMDS (1M in THF; 2 eq) is added to a cold (−-10° C.) stirred solution of methyl 2-(6-oxo-2-(piperidin-1-yl)-4-p-tolyl-1,6-dihydropyrimidin-5-yl)pentanoate (1 eq) in dry DMF (2 mL/mmol of the limiting reagent). After stirring for 5 minutes, benzyl bromide (2 eq) is added and the reaction mixture is stirred at room temperature for 18 hours. A saturated solution of ammonium chloride is then added and the aqueous layer is extracted with ethyl acetate. The organic layer is dried over magnesium sulphate, filtered and evaporated to dryness. The crude material is purified by flash chromatography on silica gel to provide the methyl 2-(1-benzyl-6-oxo-2-(piperidin-1-yl)-4-p-tolyl-1,6-dihydropyrimidin-5-yl)pentanoate which is deprotected following general method D yielding to the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906906B2
Source datasetuspto-grants-2014_12
ORD IDord-b27097ad1a784ca2b62a04aa35cbea39
Source noteuspto-grants-2014_12