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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 732716Erstellt: 25. Oktober 2026

1,1-Dichloroethane → 4-(Methoxycarbonyl)phenyl(3s,4s)-3-({[1-(1-benzothien-3-yl)ethyl]amino}methyl)-4-phenylpyrrolidine-1-carboxylate

https://huagongshe.com/reaction/732716

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1-DichloroethaneHCID 6365—
Edukt3-AcetylbenzothiopheneHCID 14316—
EduktSodium borohydrideHCID 4311764—
EduktHCID 68911676HCID 68911676—
KatalysatorHCID 178460666HCID 178460666—
LösungsmittelMethanolHCID 887—
Produkt4-(Methoxycarbonyl)phenyl(3s,4s)-3-({[1-(1-benzothien-3-yl)ethyl]amino}methyl)-4-phenylpyrrolidine-1-carboxylateHCID 6891158155%

Reaktionsschritte

A 1.0 ml dichloroethane solution of 119 mg of 4-(methoxycarbonyl)phenyl(3S,4S)-3-(aminomethyl)-4-phenylpyrrolidine-1-carboxylate and 62 mg of 3-acetylbenzothiophene was mixed with 0.12 ml of tetraisopropoxy titanium and stirred for 2 hours. The reaction solution was diluted with 1.0 ml of methanol, mixed with 38 mg of sodium borohydride, further stirred for 1 hour and then concentrated under a reduced pressure, and the thus obtained was purified by a silica gel chromatography (chloroform-methanol) to obtain 95 mg of 4-(methoxycarbonyl)phenyl(3S,4S)-3-({[1-(1-benzothien-3-yl)ethyl]amino}methyl)-4-phenylpyrrolidine-1-carboxylate as a yellow amorphous substance. EP: 515.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07585886B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-4b019befc9854dcc9b2ccdf87093c635
Quellennotizuspto-grants-2009_09