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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968643Generated: October 28, 2026

Pyridine → Phenyl 4-(3-ethynylphenylamino)quinazolin-6-ylcarbamate

https://huagongshe.com/reaction/1968643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenyl chloroformateHCID 15891—
ReactantN4-(3-Ethynylphenyl)quinazoline-4,6-diamineHCID 11492625—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductPhenyl 4-(3-ethynylphenylamino)quinazolin-6-ylcarbamateHCID 5914277295%

Reaction Steps

To a solution of N4-(3-ethynylphenyl)quinazoline-4,6-diamine (100 mg, 0.38 mmol) in DMF (2 mL) containing pyridine (37 μL, 0.46 mmol) was added phenyl chloroformate (49 μL, 0.38 mmol) dropwise at room temperature for 1 h. The reaction mixture was diluted with ethyl acetate and washed with water and brine. The combined organic layers were concentrated to give phenyl 4-(3-ethynylphenylamino)quinazolin-6-ylcarbamate as a yellow solid in 95% yield and used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426430B2
Source datasetuspto-grants-2013_04
ORD IDord-ba8e2a5a68de4adeab1bb0f2a5c12bcf
Source noteuspto-grants-2013_04