HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1788759Erstellt: 25. Oktober 2026
Triethylamine → 3-(Pyridine-3-carbonyl)-1,3-thiazolidine-4-carboxylic acid
https://huagongshe.com/reaction/1788759
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Timonacic | HCID 9934 | — |
| Edukt | 3-Pyridinecarbonyl chloride, hydrochloride (1:1) | HCID 88438 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | 3-(Pyridine-3-carbonyl)-1,3-thiazolidine-4-carboxylic acid | HCID 13375478 | 56,4% |
Reaktionsschritte
Nicotinoyl chloride hydrochloride (534 g) is added over 1 hour at a temperature of between 30° and 52° C. to a solution of thiazolidine-4-carboxylic acid (400 g) and triethylamine (613 g) in chloroform (4,500 cc). The solution obtained is heated at a temperature of about 64° C. for 4 hours. After stirring at a temperature of about 20° C. for 16 hours, the crystals which have appeared are separated off by filtration, washed 3 times with chloroform (1,500 cc in total), then 3 times with diethyl ether (1,500 cc in total) and are dried under reduced pressure (20 mm Hg; 2.7 kPa) at a temperature of about 20° C. in the presence of potassium hydroxide pellets. N-nicotinoylthiazolidine-4-carboxylic acid (403 g) is thus obtained in the form of white crystals melting at 190° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04684658 |
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| Quelldatensatz | uspto-grants-1987_08 |
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| ORD ID | ord-47cc5b7ec62c400e8d9aa5bf0052b74e |
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| Quellennotiz | uspto-grants-1987_08 |
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