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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 264703Erstellt: 26. Oktober 2026

Acetic Acid → (2R*,4S*)-2-benzyl-1-(3,5-dichlorobenzoyl)-N-diphenylmethyl-4-piperidinamine

https://huagongshe.com/reaction/264703

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktBenzophenoneHCID 3102—
EduktSodium cyanoborohydrideHCID 5003444—
Edukt2-Benzyl-1-(3,5-dichlorobenzoyl)-4-piperidinamineHCID 21220201—
LösungsmittelTolueneHCID 1140—
Produkt(2R*,4S*)-2-benzyl-1-(3,5-dichlorobenzoyl)-N-diphenylmethyl-4-piperidinamineHCID 57170253—

Reaktionsschritte

A solution of 200 mg (0.551 mmol) of (2R*,45*)-2-benzyl-1-(3,5-dichlorobenzoyl)-4-piperidinamine and 110 mg (0.606 mmol) of benzophenone in 5 ml of toluene are kept at reflux for 18 hours. The reaction mixture is then concentrated in a rotary evaporator and dissolved in 3 ml of methanol, and 69 mg (1.10 mmol) of sodium cyanoborohydride are added at RT. The reaction mixture is adjusted to pH=5 with 80 μl of acetic acid and stirred at RT for 68 hours. The title compound ##STR98## is obtained as white foam (120 mg, 41%). TLC:toluene/ethyl acetate (7:3) Rf =0.79, FD-MS:M+ =528, 530; IR:1630 cm-1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05646144
Quelldatensatzuspto-grants-1997_07
ORD IDord-ffd66f18dc844192b04fcf55fc735a75
Quellennotizuspto-grants-1997_07