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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 223501Erstellt: 25. Oktober 2026

N-(2-amino-2-methylpropyl)-2-phenylacetamide → 1-(4-Amino-3,5-dichlorophenyl)-2-[1,1-dimethyl-2-(2-phenylacetamido)ethylamino]ethanol dihydrochloride

https://huagongshe.com/reaction/223501

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-(2-amino-2-methylpropyl)-2-phenylacetamideHCID 12876178—
Edukt4-Amino-3,5-dichlorophenylglyoxal hydrateHCID 20521529—
LösungsmittelMethanolHCID 887—
Produkt1-(4-Amino-3,5-dichlorophenyl)-2-[1,1-dimethyl-2-(2-phenylacetamido)ethylamino]ethanol dihydrochlorideHCID 70540304130,4%

Reaktionsschritte

A mixture of 4-amino-3,5-dichlorophenylglyoxal hydrate (1.18 g.) and 1,1-dimethyl-2-(2-phenylacetamido)ethylamine (1.03 g.) in methanol (20 ml.) was stirred at room temperature for 16 hours. The mixture was then filtered and the filtrate stirred vigorously during the dropwise addition of a solution of sodium borohydride (500 mg.) in water (2 ml.). After stirring for 2 hours, the mixture was acidified with concentrated hydrochloric acid to pH 2-3, and then evaporated. The solid residue was suspended in water (50 ml.) and the suspension obtained was extracted with ether (100 ml). The aqueous phase was basified to pH 12-13 by addition of aqueous ammonia solution (density 0.88), and extracted with ether (2×100 ml.). The combined extracts were dried (MgSO4) and evaporated. The resultant oil was dissolved in propan-2-ol (5 ml.) and an ethereal solution of hydrogen chloride was added to bring the pH to 2-3. Further addition of an excess of dry ether gave a precipitate (1.05 g., 43%) of 1-(4-amino-3,5-di-chlorophenyl)-2-[1,1-dimethyl-2-(2-phenylacetamido)ethylamino]-ethanol dihydrochloride (Example 1), m.p. 105°-8° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04355045
Quelldatensatzuspto-grants-1982_10
ORD IDord-337f585733a14e62b6f91769aa7e30d9
Quellennotizuspto-grants-1982_10