Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 51962Erstellt: 24. Oktober 2026

Pyridine → HCID 86585942, Verbindung

https://huagongshe.com/de/reaction/51962

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktThionyl ChlorideHCID 24386—
EduktHCID 964395HCID 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
PatentnummerUS06713489B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-7c6d04060e1e4a2cb55986e17a5d12d7
Quellennotizuspto-grants-2004_03