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
Participants
| Role | Name | HCID | Charge |
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| Reactant | L-(+)-Cysteine | HCID 5862 | — |
| Reactant | 3-Pyridinecarboxaldehyde | HCID 10371 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(3-Piridyl)thiazolidine-4-carboxylic acid | HCID 327593 | 80,855% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05120751 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-483e5aa794964bf7a81c912380198b5b |
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| Source note | uspto-grants-1992_06 |
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