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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 22223Erstellt: 26. Oktober 2026

Cysteamine → 2-(2-Chloro-5-pyridyl)thiazolidine

https://huagongshe.com/reaction/22223

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCysteamineHCID 6058—
Edukt6-Chloropyridine-3-carbaldehydeHCID 2764053—
LösungsmittelBenzeneHCID 241—
Produkt2-(2-Chloro-5-pyridyl)thiazolidineHCID 1375278989,9%

Reaktionsschritte

A solution composed of 6-chloronicotinaldehyde (14.2 g), 2-aminoethanethiol (7.7 g) and benzene (80 ml) was heated with stirring for 5 hours while removing water as an azeotrope. After the reaction, benzene was distilled off under reduced pressure, and further volatile materials were removed at 1 mmHg and 70° C. to give 2-(2-chloro-5-pyridyl)thiazolidine (18 g) as a residue. Ten grams of 2-(2-chloro-5-pyridyl)thiazolidine was dissolved in 100 ml of ethanol, and sodium borohydride was added. With stirring, the mixture was gradually heated and thereafter refluxed for 1 hour. Ethanol was distilled off under reduced pressure, and chloroform was added to the residue. Insoluble materials were separated by filtration and the chloroform layer was washed with water and dehydrated. Chloroform was distilled off under reduced pressure to give the desired N-(2-chloro-5-pyridylmethyl)2-aminoethanethiol (8.3 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05428032
Quelldatensatzuspto-grants-1995_06
ORD IDord-55ad2e916fc14fdc96af4991eedb5385
Quellennotizuspto-grants-1995_06