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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827266Generated: November 1, 2026

1-Methylimidazole → HCID 10183987, compound

https://huagongshe.com/reaction/1827266

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylimidazoleHCID 1390—
ReactantChlorotriethylsilaneHCID 13819—
ReactantHCID 22136465HCID 22136465—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10183987HCID 1018398740%

Reaction Conditions

Temperature-70 °C

Reaction Steps

BuLi (2.9 ml;0.0046 mol) was added dropwise at −70° C. to a solution of 1-methyl-1H-imidazole (0.0046 mol) in THF (7 ml) under N2 flow. The mixture was stirred at −70° C. for 15 min. Chlorotriethyl-silane (0.0048 mol) was added. The mixture was stirred at −70° C. for 15 min. n BuLi (2.6 ml;0.0041 mol) was added dropwise. The mixture was stirred at −70° C. for 15 min. A solution of intermediate (4) (0.00264 mol) obtained in Example A2, in THF (20 ml) was added dropwise at −70° C. The mixture was stirred at −70° C. for 1 hour, poured out into ice water and extracted with EtOAc. The organic layer was separated, dried (MgSO4), filtered, and the solvent was evaporated. The residue (2.1 g) was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH; 95/5/0.2; 15–40 μm). The pure fractions were collected and the solvent was evaporated. The residue (0.59 g) was crystallized from diethylether. The precipitate was filtered off and dried, yielding 0.49 g (40%) of 4-(3-chlorophenyl)-α-(4-chlorophenyl)-2-methyl-α-(1-methyl-1H-imidazol-5-yl)-6-quinazolinemethanol, mp. 223° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053105B2
Source datasetuspto-grants-2006_05
ORD IDord-92f260d024094b71853b6319d1a6fd1c
Source noteuspto-grants-2006_05