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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2956Erstellt: 23. Oktober 2026

1-(2-Chloroethyl)piperidine → 2-(2-Chlorophenyl)-4-(piperidin-1-yl)butanenitrile

https://huagongshe.com/de/reaction/2956

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(2-Chloroethyl)piperidineHCID 74827—
Edukt(o-Chlorophenyl)acetonitrileHCID 76112—
Produkt2-(2-Chlorophenyl)-4-(piperidin-1-yl)butanenitrileHCID 11043596—

Reaktionsschritte

The present invention relates to a novel process for the preparation of N-heterocyclealkanamide derivatives having the following formula: ##STR1## which comprises reacting 1-(2-chloroethyl)piperidine with 2-chlorobenzeneacetonitrile to give (±)-α-(2-chlorophenyl)-1-piperidinebutanenitrile; alkylating the piperidenebutanenitrile to give (±)-α-(2-chlorophenyl)-α-(2,2-dimethoxyethyl)piperidine-1-butanenitrile; hydrolyzing the resulting alkylated piperidinebutanenitrile to give (±)-α-(2-chlorophenyl)-α-(2-oxoethyl)piperidine-1-butanenitrile; reacting the resulting piperidinebutanenitrile with isopropylamine to form (±)-α-(2-chlorophenyl)-α-[2-[(1-methylethyl)imino]ethyl]piperidine-1-butanenitrile; reducing the resulting imine to form (±)-α-(2-chlorophenyl)-α-[2-[(1-methylethyl)amino]ethyl]-piperidine-1-butanenitrile; acetylating the resulting amine to form (±)-N-[3-(2-chlorophenyl)-3-cyano-5-(1-piperidinyl)pentyl]-N-(1-methylethyl)acetamide; hydrolyzing the resulting acetylated amino substituted piperidine butanenitrile to form (±)-α-[2-[acetyl(1-methylethyl)amino]ethyl]-α-(2-chlorophenyl)-1-piperidinebutanamide; and isolating the resulting piperidinebutanamide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05731435
Quelldatensatzuspto-grants-1998_03
ORD IDord-bdf0ab77d0b64f258945b0b094a91458
Quellennotizuspto-grants-1998_03