Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276501Erstellt: 24. Oktober 2026

Ethanolamine → N-((1S)-1-(benzylthiomethyl)-2-chloroethyl)-N-isobutylammonium chloride

https://huagongshe.com/de/reaction/276501

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolamineHCID 700—
EduktThionyl ChlorideHCID 24386—
Edukt1,3-OxazolidineHCID 536683—
Edukt(1S)-1-(Benzylthiomethyl)-2-hydroxyethylamineHCID 2817366—
Edukt(4S)-2-isopropyl-4-(benzylthiomethyl)-1,3-oxazolidineHCID 57283350—
EduktN-((1S)-1-(benzylthiomethyl)-2-hydroxyethyl)-N-isobutylamineHCID 69992249—
ProduktN-((1S)-1-(benzylthiomethyl)-2-chloroethyl)-N-isobutylammonium chlorideHCID 69993869—

Reaktionsschritte

(1S)-1-(Benzylthiomethyl)-2-hydroxyethylamine was made from (L)-S-benzylcysteine methyl ester as described in Method B1b. The 2-hydroxyethylamine was converted to (4S)-2-isopropyl-4-(benzylthiomethyl)-1,3-oxazolidine according to Method B4c, Step 1. The oxazolidine was reduced to N-((1S)-1-(benzylthiomethyl)-2-hydroxyethyl)-N-isobutylamine according to Method B4c, Step 2. The resulting 2-hydroxyethylamine was treated with SOCl2 according to Method B7c to give N-((1S)-1-(benzylthiomethyl)-2-chloroethyl)-N-isobutylammonium chloride. 2-Ethyl-4-cyanophenyl isothiocyanate was reacted with N-((1S)-1-(benzylthiomethyl)-2-chloroethyl)-N-isobutylammonium chloride according to Method C1b to give (4S)-2-(2-ethyl-4-cyanophenylimino)-4-(benzylthiomethyl)-3-isobutyl-1,3-thiazolidine HCl salt.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06353006B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-79208f749d0e4332944ea4e565a6e6f7
Quellennotizuspto-grants-2002_03