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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 841825Erstellt: 25. Oktober 2026

Pyridine → HCID 86585942, Verbindung

https://huagongshe.com/reaction/841825

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktThionyl ChlorideHCID 24386—
Edukt2-(Benzyloxy)-3-methoxybenzoic acidHCID 964395—
Edukt7-Amino-quinoline-3-carboxylic acid (di-pyridin-2-yl-methyl)-amideHCID 86585940—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelChloroformHCID 6212—
ProduktHCID 86585942HCID 8658594234%

Reaktionsschritte

A mixture of 2-benzyloxy-3-methoxybenzoic acid (109 mg, 0.42 mmol), thionyl chloride (5 ml) and 1 drop dimethylformamide was heated under reflux for 2 hr. The thionyl chloride was removed in vacuo, with traces being removed by adding methylene chloride and concentrating the solution in vacuo. The resulting 2-benzyloxy-3-methoxybenzoyl chloride was dissolved in chloroform and the solution was added dropwise to a solution of 7-amino-quinoline-3-carboxylic acid (di-pyridin-2-yl-methyl)-amide (75 mg, 0.21 mmol), 4-(N,N-dimethylaminopyridine) (DIMAP) (3 mg, 0.02 mmol) and pyridine (0.068 ml, 0.84 mmol) in chloroform at room temperature. The resulting solution was heated under reflux for 3 hr, then cooled to room temperature and concentrated to dryness in vacuo. The residue was dissolved in ethyl acetate, washed sequentially with water and brine, dried over anhydrous sodium sulfate and concentrated to dryness in vacuo. The residue (960 mg) was purified by column chromatography on silica gel, eluting with 98:2 chloroform/methanol to yield the title compound as a solid (40.3 mg, 34% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06369075B1
Quelldatensatzuspto-grants-2002_04
ORD IDord-d53ac1cdca504b87a9b25e5bf200ceec
Quellennotizuspto-grants-2002_04