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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490265Generated: October 29, 2026

Imidazole → HCID 10000618, compound

https://huagongshe.com/reaction/490265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantTriethylamineHCID 8471—
Reactant3-Benzyl-2-(1-bromo-2-methylpropyl)-7-chloroquinazolin-4(3H)-oneHCID 21097058—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
ProductHCID 10000618HCID 1000061816%

Reaction Steps

To a solution of (±)-3-benzyl-2-(1-bromo-2-methyl-propyl)-7-chloro-3H-quinazolin-4-one (a compound of Formula 105, 250 mg, 0.616 mmol) in DMF (3 mL) was added triethylamine (0.130 mL, 0.924 mmol) and imidazole (63.0 mg, 0.924 mmol) followed by tetrabutylammonium iodide (228 mg, 0.616 mmol). The resultant solution was heated to 90° C., stirred for 18 h and allowed to cool to room temperature. The reaction mixture was quenched with water (3 mL) and diluted with ether (10 mL). The aqueous layer was extracted with ether (10 mL) ad the combined extracts were dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography (1:1 hexanes:ethyl acetate) to provide 38 mg (16%) of the title compound as a yellow solid. MS(ES+) m/e 393.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528137B2
Source datasetuspto-grants-2009_05
ORD IDord-ed32b4add5b64d8b8e50b0a685c5a26a
Source noteuspto-grants-2009_05