Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777704Generated: November 1, 2026

Aniline → (S)-tert-butyl 1-(5-chloro-4-oxo-3-phenyl-3,4-dihydroquinazolin-2-yl)ethylcarbamate

https://huagongshe.com/reaction/1777704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantDiphenyl phosphiteHCID 62550—
Reactant2-Amino-6-chlorobenzoic acidHCID 75071—
ReactantTert-butoxycarbonylalanineHCID 85082—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
Product(S)-tert-butyl 1-(5-chloro-4-oxo-3-phenyl-3,4-dihydroquinazolin-2-yl)ethylcarbamateHCID 86686186—

Reaction Conditions

Temperature40 °C

Reaction Steps

Diphenyl phosphonate (1.9 mL, 10 mmol) was added to a solution of 2-amino-6-chlorobenzoic acid (495 mg, 2.9 mmol) and (S)-2-(tert-butoxycarbonylamino)propanoic acid (710 mg, 3.77 mmol) in pyridine (3 mL). The reaction mixture was stirred at 40° C. for 2 hours. Aniline (274 mg, 3.48 mmol) was then added to the reaction mixture, which was then stirred at 55° C. for 12 hours. The reaction mixture was cooled to room temperature. This mixture was then diluted with EtOAc (50 mL), washed with 1N aqueous HCl (2×50 mL), brine (50 mL), and dried over sodium sulfate. The organics layer was filtered and concentrated in vacuuo to afford material which was purified by column chromatography on SiO2 eluting with EtOAc in hexanes (0-50%) to afford (S)-tert-butyl 1-(5-chloro-4-oxo-3-phenyl-3,4-dihydroquinazolin-2-yl)ethylcarbamate as a solid. ES/MS m/z=400.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266878B2
Source datasetuspto-grants-2016_02
ORD IDord-b71ea420da334ef59292ab9ee6e6630a
Source noteuspto-grants-2016_02