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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 597242Erstellt: 26. Oktober 2026

Pyridine → 3,4,5-Trimethoxybenzeneacetyl-1-[(3,4-dimethoxyphenyl)-methylene]isoquinoline

https://huagongshe.com/reaction/597242

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktDiisopropylethylamineHCID 81531—
Edukt2-(3,4,5-trimethoxyphenyl)acetyl ChlorideHCID 11032124—
Edukt3,4-Dihydro-6,7-dimethoxy-1-[(3,4-dimethoxyphenyl)methylene]isoquinolineHCID 68123391—
LösungsmittelBenzeneHCID 241—
LösungsmittelChloroformHCID 6212—
Produkt3,4,5-Trimethoxybenzeneacetyl-1-[(3,4-dimethoxyphenyl)-methylene]isoquinolineHCID 86734573—

Reaktionsschritte

To a suspension of 12 parts of 3,4-dihydro-6,7-dimethoxy-1-[(3,4-dimethoxyphenyl)methylene]isoquinoline in 50 parts of pyridine and 5 parts of N-ethyl-N-(1-methylethyl)-2-propanamine is added a solution of 10 parts of 3,4,5-trimethoxybenzeneacetyl chloride in 45 parts of benzene. The resultant mixture is heated at the boiling point under reflux for 1 hour, then cooled and thereupon diluted with 500 parts of chloroform. The resultant solution is washed with water, dried over anhydrous sodium sulfate, and stripped of solvent by vacuum distillation. The residue is crystallized from a mixture of ethyl acetate and ether to give (Z)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-(3,4,5-trimethoxybenzeneacetyl-1-[(3,4-dimethoxyphenyl)-methylene]isoquinoline melting at 164°-170°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04013666
Quelldatensatzuspto-grants-1977_03
ORD IDord-9277f6817e6345548df65511f3cdca40
Quellennotizuspto-grants-1977_03