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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1056076Erstellt: 26. Oktober 2026

Aniline → 8-bromo-N-phenylquinazolin-2-amine

https://huagongshe.com/reaction/1056076

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAnilineHCID 6115—
EduktAmmonium ChlorideHCID 25517—
EduktLithium HexamethyldisilazideHCID 2733832—
Edukt8-Bromo-2-chloroquinazolineHCID 45790061—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt8-bromo-N-phenylquinazolin-2-amineHCID 89781929100%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

LHMDS (1.0M in THF; 4.11 mL, 4.11 mmol) was added to a solution of 8-bromo-2-chloroquinazoline (Ark Pharm, Inc., Libertyville, Ill.; 500 mg, 2.053 mmol) and aniline (0.337 mL, 3.70 mmol) in THF (10 mL) at 0° C., and the resulting solution was stirred at 0° C. for 10 min. Saturated aq. NH4Cl (10 mL) was added, and the resulting mixture was partitioned between EtOAc (50 mL) and additional saturated aq. NH4Cl (30 mL). The organic layer was separated, washed with brine (30 mL), dried over Na2SO4, filtered and concentrated in vacuo. Chromatographic purification of the residue (silica gel, 0-10% MeOH/DCM) furnished 8-bromo-N-phenylquinazolin-2-amine (616 mg, 2.052 mmol, 100% yield) as a yellow solid: m/z (ESI, +ve) 300.0 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09394297B2
Quelldatensatzuspto-grants-2016_07
ORD IDord-186b83400f264668b58b6ad833df54ab
Quellennotizuspto-grants-2016_07