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HRID 22223作成日:2026年10月27日

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

https://huagongshe.com/reaction/22223

反応式

関与物質

役割名称HCID仕込み量
反応物CysteamineHCID 6058—
反応物6-Chloropyridine-3-carbaldehydeHCID 2764053—
溶媒BenzeneHCID 241—
生成物2-(2-Chloro-5-pyridyl)thiazolidineHCID 1375278989.9%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05428032
出典データセットuspto-grants-1995_06
ORD IDord-55ad2e916fc14fdc96af4991eedb5385
出典メモuspto-grants-1995_06