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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67776Generated: October 29, 2026

Methylamine → 4-(4-Chloro-3-methylsulfamoylphenyl)-2-(4-methoxyphenylimino)-3-methyl-4-thiazoline hydrochloride

https://huagongshe.com/reaction/67776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant4-(4-Chloro-3-chlorosulfonylphenyl)-2-(4-methoxyphenyl-imino)-3-methylthiazolidin-4-ol hydrobromideHCID 86738555—
SolventMethanolHCID 887—
Product4-(4-Chloro-3-methylsulfamoylphenyl)-2-(4-methoxyphenylimino)-3-methyl-4-thiazoline hydrochlorideHCID 20527120—

Reaction Steps

10.6 g (0.02 mole) of 4-(4-chloro-3-chlorosulfonylphenyl)-2-(4-methoxyphenyl-imino)-3-methylthiazolidin-4-ol hydrobromide are introduced into a mixture of 10 ml of 40% strength aqueous methylamine and 150 ml of methanol and the resulting mixture is stirred for 20 hours at room temperature. The solvent is distilled off, the residue is taken up in 100 ml of ethanol and this solution is acidified with methanolic or ethanolic hydrogen chloride solution and heated at the boil for 2 hours. The solvent is distilled off, the residue is crystallized under ether, ethyl acetate or diisopropyl ether and the crystals are filtered off. Melting point 257° C. (with decomposition) (from isopropanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04346088
Source datasetuspto-grants-1982_08
ORD IDord-bf2cde96df4644e89bf9139cab4d6fe7
Source noteuspto-grants-1982_08