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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1734740Erstellt: 25. Oktober 2026

Ethylenediamine → Lazabemide

https://huagongshe.com/reaction/1734740

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylenediamineHCID 3301—
Edukt2,5-DichloropyridineHCID 27685—
EduktSodium MethoxideHCID 10942334—
Katalysator1,3-Bis(diphenylphosphino)propaneHCID 81219—
ProduktHydrochloric AcidHCID 313—
ProduktLazabemideHCID 7130775%

Reaktionsschritte

The amidation of 5 g (33.8 mmol) of 2,5-dichloropyridine in the presence of 12.1 g (202 mmol) of ethylenediamine, 8.8 mg of palladium-dichloro-bis(acetonitrile) and 21 mg of 1,3-bis(diphenylphosphino)propane is carried out at 110° in a manner analogous to Example 1. After the addition of 1.91 g (35.5 mmol) of sodium methylate and evaporation of the reaction mixture there are obtained, by extraction with 3N hydrochloric acid and subsequent basification of the acidic-aqueous solution, 5.05 g (75%) of N-(2-aminoethyl)-5-chloropyridine-2-carboxamide; content according to HPLC: 98.2 wt. %, content of N,N'-ethylene-bis(5-chloro-2-pyridinecarboxamide): <1% (GC). Conversion of the free base with hydrogen chloride in methanol into the hydrochloride and crystallization from methanol/ether yields N-(2-aminoethyl)-5-chloropyridine-2-carboxamide hydrochloride as white crystals, m.p. 191°-195°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05534635
Quelldatensatzuspto-grants-1996_07
ORD IDord-d86ab5eb913a4cbaa8df05195cf4826c
Quellennotizuspto-grants-1996_07