Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702265Generated: October 30, 2026

Cysteamine Hydrochloride → HCID 178494333, compound

https://huagongshe.com/reaction/1702265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCysteamine HydrochlorideHCID 9082—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium MethoxideHCID 10942334—
Reactant2-(Chloromethyl)-4-methyl-1,3-thiazoleHCID 11275091—
Reactant3,4-Dimethoxy-1,2,5-thiadiazole 1,1-dioxideHCID 12230538—
Reactant(4-Methyl-1,3-thiazol-2-yl)methanolHCID 17750909—
ProductHCID 178494333HCID 178494333—

Reaction Steps

When 2-chloromethyl-4-methylthiazole [prepared by the reaction of thionyl chloride and 2-hydroxymethyl-4-methylthiazole, which itself is prepared according to the procedure of J. Chem. Soc., (Suppl. Issue No. 1), S106-111 (1966) or Acta Chem.Scand., 20, 2649 (1966)] is reacted with cysteamine hydrochloride and about two equivalents of a strong base such as sodium methoxide, and the resultant amine is treated with 3,4-dimethoxy-1,2,5-thiadiazole 1,1-dioxide, there is produced 3-methoxy-4-{2-[(4-methylthiazol-2-yl)methylthio]ethylamino}-1,2,5-thiadiazole 1,1-dioxide. When the latter compound is reacted with methylamine according to the general procedure of Example 31, there is produced 3-methylamino-4-{2-[(4-methylthiazol-2-yl)methylthio]ethylamino}-1,2,5-thiadiazole 1,1-dioxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04380638
Source datasetuspto-grants-1983_04
ORD IDord-4b6a937142154d85ad736abefb1c9dd4
Source noteuspto-grants-1983_04