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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276473Erstellt: 24. Oktober 2026

Ethanolamine → (4S)-2-(4-cyanophenylimino)-3,4-diisobutyl-1,3-thiazolidine

https://huagongshe.com/de/reaction/276473

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolamineHCID 700—
EduktBenzonitrile, 4-isothiocyanato-HCID 17626—
EduktIsobutylaminehydrochlorideHCID 21133—
Edukt(+)-L-Leucine methyl esterHCID 65105—
EduktL-LeucinolHCID 111307—
Edukt(2S)-4-methyl-2-(isobutylamino)pentanolHCID 22951222—
Produkt(4S)-2-(4-cyanophenylimino)-3,4-diisobutyl-1,3-thiazolidineHCID 59113105—

Reaktionsschritte

(1S)-1-(Hydroxymethyl)-3-methylbutylamine was made from (L)-leucine methyl ester as described in Method B1b. The 2-hydroxyethylamine was converted to (2S)-4-methyl-2-(isobutylamino)pentan-1-ol as described in Method B4c. The resulting 2-hydroxyethylamine was converted to N-(1S)-1-(chloromethyl)-3-methylbutyl)-N-(isobutyl)ammonium chloride according to Method B7c. 4-Cyanophenyl isothiocyanate was reacted with N-(1S)-1-(chloromethyl)-3methylbutyl)N-(isobutyl)ammonium chloride to Method C1f to afford (4S)-2-(4-cyanophenylimino)-3,4-diisobutyl-1,3-thiazolidine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06353006B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-32ca457788204c2ab29892b4b74f8519
Quellennotizuspto-grants-2002_03