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HRID 446910作成日:2026年10月26日

Dicyclohexylcarbodiimide → (R)-benzyl 1-(6-(3-chlorophenylamino)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-3-yl)ethylcarbamate

https://huagongshe.com/reaction/446910

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物3-Chlorophenyl isothiocyanateHCID 75449—
反応物HCID 178462184HCID 178462184—
溶媒EthanolHCID 702—
溶媒Diethyl EtherHCID 3283—
生成物(R)-benzyl 1-(6-(3-chlorophenylamino)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-3-yl)ethylcarbamateHCID 8664229548.7%

反応条件

温度80 °C

反応手順

(Step 8-ii) A mixture of (R)-benzyl 1-(5-mercapto-4-amino-4H-1,2,4-triazol-3-yl)ethylcarbamate (1.32 g, 4.5 mmol) in ethanol (15 mL) was heated to 80° C. and 3-chlorophenylisothiocyanate (1.3 g, 7.65 mmol) and dicyclohexylcarbodiimide (1.11 g, 5.4 mmol) were added. After 4 hours, the reaction was cooled, diluted with an equal volume of ether, and filtered. The filter cake was washed with additional ether and the collected solids dried in vacuo to provide 0.94 g of (R)-benzyl 1-(6-(3-chlorophenylamino)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-3-yl)ethylcarbamate: ESMS MH+=429.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481538B2
出典データセットuspto-grants-2013_07
ORD IDord-99b478e2c89843c2a1f93812d9885667
出典メモuspto-grants-2013_07