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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276431Erstellt: 25. Oktober 2026

Ethanolamine → 2-(3-Quinolylimino)-3,5-diisobutyl-1,3thiazolidine

https://huagongshe.com/reaction/276431

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolamineHCID 700—
Edukt3-AminoquinolineHCID 11375—
EduktIsobutylaminehydrochlorideHCID 21133—
Edukt(+)-L-Leucine methyl esterHCID 65105—
EduktL-LeucinolHCID 111307—
Edukt3-IsothiocyanatoquinolineHCID 13718421—
Edukt(2S)-4-methyl-2-(isobutylamino)pentanolHCID 22951222—
Produkt2-(3-Quinolylimino)-3,5-diisobutyl-1,3thiazolidineHCID 18316332—

Reaktionsschritte

3-Aminoquinoline was converted to 3-quinoline isothiocyanate according to Method A2c. (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)pentanol as described in Method B4c, Steps 1-2. The alcohol was converted to N-(1S)-1-(chloromethyl)-3-methylbutyl)-N-(isobutyl)ammonium chloride as described in Method B7c. 3-Quinoline isothiocyanate was reacted with N-(1S)-1-(chloromethyl)-3-methylbutyl)-N-(isobutyl)ammonium chloride according to Method C1f to give 2-(3-quinolylimino)-3,5-diisobutyl-1,3thiazolidine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06353006B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-5ef769350033476a90dd5eeb24076b1d
Quellennotizuspto-grants-2002_03