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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276449Erstellt: 24. Oktober 2026

2,6-Dimethyl-4-nitroaniline → HCID 178428753, Verbindung

https://huagongshe.com/de/reaction/276449

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,6-Dimethyl-4-nitroanilineHCID 28159—
EduktL-LeucinolHCID 111307—
Edukt2,6-Dimethyl-4-nitrophenyl isothiocyanateHCID 12462431—
ProduktHCID 178428753HCID 178428753—

Reaktionsschritte

(1S)-1-(Hydroxymethyl)-3-methylbutylamine was converted to (1S)-1-(chloromethyl)-3-methylbutanammonium chloride as described in Method B7a. 2,6-Dimethyl-4-nitroaniline was converted into 2,6-dimethyl-4-nitrophenyl isothiocyanate according to Method A2b. 2,6-Dimethyl-4-nitrophenyl isothiocyanate was reacted with (1S)-1-(chloromethyl)-3-methylbutanammonium chloride according to Method C1a to give (4S)-2-(2-methyl-4-nitrophenylimino)-4-isobutyl-1,3-thiazolidine. The thiazolidine was reacted with isobutyl bromide according to Method D2a to give (4S)-2-(2,6-dimethyl-4-nitrophenylimino)-3,4-diisobutyl-1,3-thiazolidine HCl salt.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06353006B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-c8f901655edd4a84821309d9759a0a3f
Quellennotizuspto-grants-2002_03