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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613726Generated: October 31, 2026

Acetic Acid → O-methyl-N-(2-chloro-5-thiazolylmethyl)-N'-nitroisourea

https://huagongshe.com/reaction/613726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium HydroxideHCID 14798—
Reactant2-Chloro-5-aminomethylthiazoleHCID 10154129—
ReactantO-methyl-N-nitroisoureaHCID 136196430—
SolventWaterHCID 962—
ProductO-methyl-N-(2-chloro-5-thiazolylmethyl)-N'-nitroisoureaHCID 13640463246%

Reaction Steps

O-methyl-N-nitroisourea (3.0 g, 0.0252 mol), acetic acid (1.5 ml, 0.0262 mol, 10.4 equivalents), and 5-(aminomethyl)-2-chlorothiazole (93% purity, 4.4 g, 0.0275 mol, 1.09 equivalents) were added to water (55 ml) in this order at 24° C. The reaction mixture was adjusted to pH 7 with 30% aqueous sodium hydroxide solution. The mixture was stirred at room temperature for 2 hours and then extracted with dichloromethane. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to provide 2.9 g (46.0% yield) of O-methyl-N-(2-chloro-5-thiazolylmethyl)-N'-nitroisourea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008363
Source datasetuspto-grants-1999_12
ORD IDord-c7a6f3442714478a8d48e5bfc1a3fa6b
Source noteuspto-grants-1999_12