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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1775943Erstellt: 25. Oktober 2026

Formaldehyde → 6-chloro-2,3,4,9-tetrahydro-2-methyl-9-(2-(piperidin-1-yl)ethyl)-1H-pyrido[3,4-b]indole

https://huagongshe.com/reaction/1775943

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
EduktTrifluoroacetic acidHCID 6422—
EduktHydrazine, (4-chlorophenyl)-, hydrochloride (1:1)HCID 71600—
EduktPiperidine, 1-(2-chloroethyl)-, hydrochlorideHCID 74826—
Edukt4,4-Diethoxy-N-methylbutan-1-amineHCID 13994547—
Edukt1-(4-Chlorophenyl)-1-(2-(piperidin-1-yl)ethyl)hydrazineHCID 66911628—
Edukt2-(5-chloro-1-(2-(piperidin-1-yl)ethyl)-1H-indol-3-yl)-N-methylethanamineHCID 66911768—
KatalysatorTetrabutylammonium ChlorideHCID 70681—
LösungsmittelAcetonitrileHCID 6342—
Produkt6-chloro-2,3,4,9-tetrahydro-2-methyl-9-(2-(piperidin-1-yl)ethyl)-1H-pyrido[3,4-b]indoleHCID 44242439—

Reaktionsschritte

The title compound was prepared by following General Methods 2, 3 and 4 using 4-chlorophenylhydrazine hydrochloride, 1-(2-chloroethyl)piperidine hydrochloride, and tetra-n-butylammonium chloride (General Method 2), 1-(4-chlorophenyl)-1-(2-(piperidin-1-yl)ethyl)hydrazine (Example 3) and 4,4-diethoxy-N-methylbutan-1-amine (General Method 3) and 2-(5-chloro-1-(2-(piperidin-1-yl)ethyl)-1H-indol-3-yl)-N-methylethanamine (Example 12), formaldehyde and TFA in acetonitrile (General Method 4).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09260429B2
Quelldatensatzuspto-grants-2016_02
ORD IDord-cb7eaa3f6d224eaa804605f35d191e6b
Quellennotizuspto-grants-2016_02