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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 379523Erstellt: 25. Oktober 2026

Phthalylglycine aldehyde → N-(2-Aminoethyl)-7,8-dimethoxy-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/379523

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhthalylglycine aldehydeHCID 76201—
Edukt7,8-Dimethoxy-1,2,3,4-tetrahydroisoquinolineHCID 179606—
EduktSodium AcetateHCID 517045—
EduktSodium triacetoxyborohydrideHCID 5049666—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(2-Aminoethyl)-7,8-dimethoxy-1,2,3,4-tetrahydroisoquinolineHCID 15884736100%

Reaktionsschritte

To a solution of 7,8dimethoxy-1,2,3,4-tetrahydroisoquinoline (421 mg, 2.2 mmol), 2-phthalimidoacetaldehyde (410 mg, 2.2 mmol) and NaOAc (180 mg, 2.2 mmol) in 27 mL of CH2Cl2 was added 690 mg (3.25 mmol) of NaBH(OAc)3 in small portions. After stirring 1 hour at room temperature, the reaction mixture was diluted with CH2Cl2 and washed with a saturated Na2CO3 solution and brine. The residue obtained after evaporation of CH2Cl2 was dissolved in 25 mL of EtOH and treated with 1.2 mL of hydrazine hydrate overnight. The reaction mixture was then filtered and evaporated to give 510 mg (100%) of the title compound; MS m/e 327 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06300316B1
Quelldatensatzuspto-grants-2001_10
ORD IDord-d1c0c9b4ab2b45c485c159650512548b
Quellennotizuspto-grants-2001_10