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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1094983Erstellt: 25. Oktober 2026

Pyridine → 2-(3-Chloromethyl-benzoylamino)-5-dipropylamino-benzoic acid methyl ester

https://huagongshe.com/reaction/1094983

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktDichloromethaneHCID 6344—
EduktVeratroyl chlorideHCID 77070—
Edukt2-Amino-5-dipropylamino-benzoic acid methyl esterHCID 61313650—
Produkt2-(3-Chloromethyl-benzoylamino)-5-dipropylamino-benzoic acid methyl esterHCID 66637743—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

2-Amino-5-dipropylamino-benzoic acid methyl ester (compound A) (243 mg) produced by the above reaction was dissolved in anhydrous methylene chloride (3.0 ml). Subsequently, pyridine (170 μl) and 3-(chloromethyl)benzoyl chloride (compound B) (166 μl) were added to the solution at 0° C., and the mixture was stirred at 0° C. for one hr. After the completion of the reaction, distilled water was added thereto, and the mixture was subjected to separatory extraction with chloroform. The organic layer was washed with saturated brine, was dried over sodium sulfate, and was then concentrated. The residue was purified by column chromatography using a hexane-acetone system to give 2-(3-chloromethyl-benzoylamino)-5-dipropylamino-benzoic acid methyl ester as a useful intermediate (280 mg, yield 64%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08134015B2
Quelldatensatzuspto-grants-2012_03
ORD IDord-c368aed5d7bb4f9cbc810a6899df9373
Quellennotizuspto-grants-2012_03