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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801959Generated: October 31, 2026

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

https://huagongshe.com/reaction/1801959

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 numberUS08349851B2
Source datasetuspto-grants-2013_01
ORD IDord-1279469355b94c5b820e756398e06945
Source noteuspto-grants-2013_01