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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233090Generated: November 1, 2026

Diethyl Ether → 2-(4-Fluorophenyl)-8-methylimidazo[1,2-a]pyrazine

https://huagongshe.com/reaction/2233090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTetrahydrofuranHCID 8028—
ReactantMethyl 2-(4-fluorophenyl)imidazo[1,2-a]pyrazine-8-carboxylateHCID 57438736—
ReactantHCID 178418689HCID 178418689—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product2-(4-Fluorophenyl)-8-methylimidazo[1,2-a]pyrazineHCID 57438749104.1%

Reaction Steps

A solution of 3M MeMgBr in Et2O (16.1 mL, 48.3 mmol) was added drop-wise to a mixture of 8-chloro-2-(4-fluorophenyl)-imidazo[1,2-a]pyrazine (prepared using general procedure B using 3-chloropyrazin-2-ylamine and 2-bromo-1-(4-fluorophenyl)-ethanone; 10.0 g, 40.6 mmol), ferric acetylacetonate (0.71 g, 2.0 mmol), THF (240 mL), and NMP (23 mL) at about 0° C. The mixture was warmed to ambient temperature over about 1 hour. After about 1 hour, the reaction was cooled to about 0° C. and treated with additional 3 M MeMgBr in Et2O (4 mL, 12 mmol). The mixture was allowed to warm to ambient temperature over about 1 h. After about an additional 1 h, the mixture was quenched with water and extracted with EtOAc. The organic layers were combined and dried with Na2SO4. After concentration, the crude material was purified by FCC on silica gel using EtOAc as an eluent to afford the expected product as an off-white solid (9.6 g, 100%): LC/MS (Table 1, Method b) Rt=1.8 min; MS m/z: 228.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709468B2
Source datasetuspto-grants-2010_05
ORD IDord-38fb06a677df4051ae93af04cc513182
Source noteuspto-grants-2010_05