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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745519Generated: October 31, 2026

Cysteamine Hydrochloride → 2-{[(Pyridin-4-yl)methyl]sulfanyl}ethan-1-amine

https://huagongshe.com/reaction/745519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCysteamine HydrochlorideHCID 9082—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 23313627HCID 23313627—
SolventEthanolHCID 702—
Product2-{[(Pyridin-4-yl)methyl]sulfanyl}ethan-1-amineHCID 13498704—

Reaction Steps

34.1 g of sodium hydroxide was dissolved in 500 ml of ethanol under an argon atmosphere and 48.6 g of 2-mercaptoethanamine hydrochloride and 35 g of 4-chloromethylpyridine pyridine hydrochloride were added with ice bath cooling. The reaction mixture was allowed to warm to room temperature over 2 hours, was concentrated, diluted with 300 ml of water and was extracted with 3×150 ml of dichloromethane. The combined organic layers were washed with 100 ml of saturated brine, dried over potassium carbonate and were evaporated to a dark oil which was distilled. The fractions bp 120°-130° C./0.1 mm amounted to 30.68 g (85%) of 2-[[(4-pyridyl)methyl]thio]ethanamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04599336
Source datasetuspto-grants-1986_07
ORD IDord-0535977a567d475a8169cd00ba652490
Source noteuspto-grants-1986_07