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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 242064Erstellt: 25. Oktober 2026

1-(p-Chlorophenyl)cyclobutanecarboxylic acid → 2-({1-[1-(4-Chlorophenyl)cyclobutyl]-4,4-dimethyl-3,4-dihydroisoquinolin-7-yl}oxy)ethanamine

https://huagongshe.com/reaction/242064

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(p-Chlorophenyl)cyclobutanecarboxylic acidHCID 602761—
Edukt2-(4-Methoxyphenyl)-2-methylpropan-1-amineHCID 3581364—
Edukt1-(4-Fluorophenyl)cyclobutanecarboxylic acidHCID 16769017—
Edukt2-({1-[1-(4-Fluorophenyl)cyclobutyl]-3,4-dihydroisoquinolin-7-yl}oxy)ethanamineHCID 58246324—
Produkt2-({1-[1-(4-Chlorophenyl)cyclobutyl]-4,4-dimethyl-3,4-dihydroisoquinolin-7-yl}oxy)ethanamineHCID 58246302—

Reaktionsschritte

2-({1-[1-(4-Chlorophenyl)cyclobutyl]-4,4-dimethyl-3,4-dihydroisoquinolin-7-yl}oxy)ethanamine was prepared analogously to 2-({1-[1-(4-fluorophenyl)cyclobutyl]-3,4-dihydroisoquinolin-7-yl}oxy)ethanamine (cf. example 65) using 2-(4-methoxyphenyl)-2-methylpropan-1-amine and 1-(4-chlorophenyl)cyclobutanecarboxylic acid in place of 2-(4-methoxyphenyl)ethanamine and 1-(4-fluorophenyl)cyclobutanecarboxylic acid, respectively.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08653100B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-89f8d178c1b24bb4a5071f72c287e11a
Quellennotizuspto-grants-2014_02