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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892799Generated: October 30, 2026

L-(+)-Cysteine → 2-(3-Piridyl)thiazolidine-4-carboxylic acid

https://huagongshe.com/reaction/892799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-(+)-CysteineHCID 5862—
Reactant3-PyridinecarboxaldehydeHCID 10371—
SolventEthanolHCID 702—
Product2-(3-Piridyl)thiazolidine-4-carboxylic acidHCID 32759380,855%

Reaction Conditions

Temperature100 °C

Reaction Steps

Cysteine (24.2 g, 0.2 mole) and 3-pyridine carboxaldehyde (21.4 g, 0.2 mmole) were suspended in 60% aqueous ethanol (400 mL) and the mixture was heated at 100° C. for 5 hours. The reaction mixture was then cooled and most of the solvent was removed in vacuo. The resulting slurry was washed with ethanol and filtered. This material was dried overnight in vacuo at 50° C. to afford the thiazolidine acid (34 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05120751
Source datasetuspto-grants-1992_06
ORD IDord-483e5aa794964bf7a81c912380198b5b
Source noteuspto-grants-1992_06