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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108849Generated: October 27, 2026

Methylamine → Nizax

https://huagongshe.com/reaction/1108849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantThiazoleHCID 9256—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Nitromethylene-thiazolidineHCID 3835583—
Reactant4-Chloromethyl-2-dimethylaminomethylthiazole dihydrochlorideHCID 18784323—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
SolventMethyl Ethyl KetoneHCID 6569—
ProductNizaxHCID 303363776.8%

Reaction Conditions

Temperature40 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06069256
Source datasetuspto-grants-2000_05
ORD IDord-ee8df60898164a978d279116049c03ba
Source noteuspto-grants-2000_05