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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613734Generated: October 30, 2026

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

https://huagongshe.com/reaction/613734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
Reactant2-Chloro-5-aminomethylthiazoleHCID 10154129—
ReactantO-methyl-N-nitroisoureaHCID 136196430—
CatalystSodium HydroxideHCID 14798—
ProductO-methyl-N-(2-chloro-5-thiazolylmethyl)-N'-nitroisoureaHCID 13640463269.4%

Reaction Steps

5-(Aminomethyl)-2-chlorothiazole (1.49 g, 10.0 mmol), was dissolved in diluted hydrochloric acid (15 ml, 10.0 mmol), and O-methyl-N-nitroisourea (1.31 g, 11.0 mmol) and sodium chloride (4.68 g, 80.0 mmol) were added. The pH was 1.9 at this time. This reaction mixture was adjusted to pH 6.2 with aqueous sodium hydroxide solution (0.1 N, 5.0 ml, 0.50 mmol) using pH meter. After 16 hours of stirring at room temperature (pH was 6.7 at this time), the resulting white crystals were collected by filtration under reduced pressure, and washed with water. The washed crystals were dried under reduced pressure (80° C., 2 hours) to provide 1.74 g (69.4% 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-aed3a4a534f6435fa517849321d9c737
Source noteuspto-grants-1999_12