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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 977047Erstellt: 24. Oktober 2026

Triethylamine → Amitriptyline

https://huagongshe.com/de/reaction/977047

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktDicyclohexylcarbodiimideHCID 10868—
EduktN-HydroxysuccinimideHCID 80170—
EduktST51005980HCID 2725051—
LösungsmittelDimethylformamideHCID 6228—
ProduktAmitriptylineHCID 2160—

Reaktionsschritte

6-Carboxyfluorescein (1.00 g, 2.66 mmol) was dissolved in 8 mL DMF, 306 mg (2.66 mmol) of N-hydroxysuccinimide (HOSu) was added, 549 mg (2.66 mmol) of 1,3-dicyclohexylcarbodiimide (DCC) was added, and the reaction stirred for 17 hours, under N2, in the dark. The reaction was then vacuum filtered, filtrate combined with 784 mg (2.65 mmol) of 2-aminoimipramine (26c), 0.56 mL (4.0 mmol) of triethylamine, and 4.0 mL DMF, and reaction allowed to stir 4 days under N2, in the dark. Reaction solvents were removed in vacuo and residue purified on reverse phase C18 preparative (1 mm) TLC plates, eluting with H2O/THF/HOAc (40/60/0.4) followed by preparative HPLC on a Waters mbondapak C18 column (19 mm×150 mm), eluting with H2O/THF/HOAc (35/65/0.4) at a flow rate of 7.0 mL/minute to yield 410 mg (24%) of the desired tracer (27) as an orange powder; mass spec (FAB) (M+H)+ 654.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05614419
Quelldatensatzuspto-grants-1997_03
ORD IDord-af4a453f212144719d9bbba75fba989f
Quellennotizuspto-grants-1997_03