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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571996Generated: October 31, 2026

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

https://huagongshe.com/reaction/571996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
Reactant2-Amino-6-chlorobenzoic acidHCID 75071—
ReactantTert-butoxycarbonylalanineHCID 85082—
ReactantDiphenoxyphosphanolateHCID 23418553—
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 phosphite (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 numberUS09029384B2
Source datasetuspto-grants-2015_05
ORD IDord-3167d46642d64bab93e6606fb0e35063
Source noteuspto-grants-2015_05