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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1108849Erstellt: 24. Oktober 2026

Methylamine → Nizax

https://huagongshe.com/de/reaction/1108849

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethylamineHCID 6329—
EduktThiazoleHCID 9256—
EduktPotassium CarbonateHCID 11430—
Edukt2-Nitromethylene-thiazolidineHCID 3835583—
Edukt4-Chloromethyl-2-dimethylaminomethylthiazole dihydrochlorideHCID 18784323—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelMethyl Ethyl KetoneHCID 6569—
ProduktNizaxHCID 303363776,8%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

A mixture of 2-nitromethylenethiazolidine (12.6 g) and acetonitrile (21.5 ml) was stirred and heated at 40° C. under argon. Methylamine (20.0 g of a 40% w/w aqueous solution) was added slowly over 30 minutes to the reaction mixture at 40° C. The mixture was cooled at ambient temperature and further methylamine (23.6 g of 40% w/w aqueous solution) was added over 2.5 hours and a solution of 4-chloromethyl-2-dimethylaminomethylthiazole dihydrochloride (25.0 g) in water (30 ml) was added over 5.5 hours with the addition of the thiazole starting simultaneously with the addition of the methylamine. The reaction mixture was left to stir for a further 15 minutes and then was concentrated under reduced pressure. The solid obtained was dissolved in methyl ethyl ketone (130 ml) and aqueous potassium carbonate solution (43 ml, 10% w/w). A further portion of methyl ethyl ketone and water (50 ml) was added to aid dissolution. The mixture was warmed slightly to obtain a solution. The mixture was separated and the aqueous layer was washed with methyl ethyl ketone (2×130 ml and then 1×50 ml). The combined organic layers were dried and evaporated under reduced pressure to yield crude nizatidine (approximately 25 g, 88% yield), which was shown to be 93.7% pure by HPLC. The crude solid was dissolved in dichloromethane (300 ml). The solution was washed with water (3×75 ml). The combined aqueous layer and the washings were back extracted with dichloromethane and the combined organic layers were concentrated under reduced pressure to give nizatidine (21.8 g, 76.8% yield) which was shown to be 98.3% pure by HPLC. The solid was dissolved in ethanol (45 ml) by warming on a steam bath. The solution was removed from the steam bath, treated with activated charcoal (2.3 g) and the mixture was boiled for a further 8 minutes. The mixture was hot filtered. The filtrate was cooled and filtered to give nizatidine (15.6 g, 55% yield) which was shown to be 99.7% pure by HPLC.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06069256
Quelldatensatzuspto-grants-2000_05
ORD IDord-ee8df60898164a978d279116049c03ba
Quellennotizuspto-grants-2000_05