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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 441242Erstellt: 25. Oktober 2026

Triethylamine → 1-{4-[2-(1-Pyrrolyl)benzoylamino]benzoyl}-1,2,3,4tetrahydroquinoline

https://huagongshe.com/reaction/441242

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktDiphenyl chlorophosphateHCID 75654—
Edukt2-(1H-pyrrol-1-yl)benzoic acidHCID 728521—
Edukt(4-aminophenyl)(3,4-dihydroquinolin-1(2H)-yl)methanoneHCID 2984117—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-{4-[2-(1-Pyrrolyl)benzoylamino]benzoyl}-1,2,3,4tetrahydroquinolineHCID 1059827560,5%

Reaktionsschritte

To a solution of 2-(1-pyrrolyl)benzoic acid (206 mg), diphenyl chlorophosphate (325 mg), 1-(4-aminobenzoyl}-1,2,3,4-tetrahydroquinoline (277 mg) in tetrahydrofuran (10 ml) was added triethylamine (333 mg) at 0° C. The resulting mixture was allowed to warm to ambient temperature where it was maintained for 5 hours. The solvent was evaporated and diluted with ethyl acetate and washed with water, saturated sodium bicarbonate aqueous solution and brine. The organic layer was dried over sodium sulfate and concentrated to give 1-{4-[2-(1-pyrrolyl)benzoylamino]benzoyl}-1,2,3,4tetrahydroquinoline (280 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05521170
Quelldatensatzuspto-grants-1996_05
ORD IDord-b85ecc7cd5d44739bc7c54ad7db59d8c
Quellennotizuspto-grants-1996_05