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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625813Generated: October 29, 2026

Ethyl 4-chloroquinazoline-2-carboxylate → HCID 86649067, compound

https://huagongshe.com/reaction/625813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-chloroquinazoline-2-carboxylateHCID 3477840—
ReactantHCID 178420691HCID 178420691—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86649067HCID 8664906737%

Reaction Conditions

Temperature-30 °C

Reaction Steps

A mixture of ethyl 4-chloroquinazoline-2-carboxylate (1 g, 4.2 mmol) in THF (50 mL) was filtered, and to the filtrate at −30° C. under Ar was added 0.5 M (3-chloro-4-fluorophenyl)magnesium bromide/THF (10.4 mL, 5.2 mmol). After stirring at −30° C. for 0.75 h, additional 0.5 M (3-chloro-4-fluorophenyl)magnesium bromide/THF (4.2 mL). After 1 h, the reaction was quenched by addition of saturated aq ammonium chloride and allowed to warm to rt. The mixture was extracted with EtOAc, and the extracts were dried over sodium sulfate, filtered, and concentrated under reduced pressure to afford (3-chloro-4-fluorophenyl)(4-chloroquinazolin-2-yl)methanone (495 mg, 37%) which was used directly in the next step. LC-MS (ESI) m/z 321 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09308207B2
Source datasetuspto-grants-2016_04
ORD IDord-ae067d957c7a4cf48f77d95f8d35362c
Source noteuspto-grants-2016_04