Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839853Generated: November 3, 2026

Hydrochloric Acid → n-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide

https://huagongshe.com/reaction/1839853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChlorineHCID 24526—
Reactant4H-1,3,5-Oxadiazin-4-imine, tetrahydro-3-methyl-N-nitro-5-[[2-(phenylthio)-5-thiazolyl]methyl]-HCID 53772588—
SolventChlorobenzeneHCID 7964—
Productn-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramideHCID 107646—

Reaction Steps

183 g of 3-(2-phenylthio-thiazol-5-yl-methyl)-5-methyl-4-nitroimino-perhydro-1,3,5-oxadiazine are introduced over a period of 5 minutes, with stirring, into a mixture of 300 g of hydrochloric acid (32%) and 150 g of chlorobenzene. 124 g of chlorine are introduced at 20° C. over a period of 4 hours. After 2 hours, excess chlorine is removed by the introduction of nitrogen, and the phases are then separated. The aqueous phase is adjusted to pH 5 with sodium hydroxide solution (30%) and then filtered, and the filtration residue is washed with water and dried in vacuo at 50° C. The title product is obtained in a purity of 97%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677457B2
Source datasetuspto-grants-2004_01
ORD IDord-3aa1e863ace94704a4d3a61c4990e288
Source noteuspto-grants-2004_01