戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 361600作成日:2026年10月26日

Phenethylamine → 4-methyl-N-phenethyl-1,2,3-thiadiazole-5-carboxamide

https://huagongshe.com/reaction/361600

反応式

関与物質

役割名称HCID仕込み量
反応物PhenethylamineHCID 1001—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物4-Methyl-1,2,3-thiadiazole-5-carboxylic acidHCID 1381992—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物4-methyl-N-phenethyl-1,2,3-thiadiazole-5-carboxamideHCID 757673694.6%

反応条件

温度5 °C

反応手順

A suspension of 9.65 g of 4-methyl-[1,2,3]thiadiazol-5-carboxylic acid in 70 ml of dichlormethane was cooled to 5° C. while stirring, treated with 0.15 g of 4-dimethylamino-pyridine and subsequently with 13.8 g of N,N'-dicyclohexyl-carbodiimide at such a rate that the internal temperature <10° C. could be maintained. After completion of the addition, the mixture was cooled to 5° C. and 8.92 g of phenethylamine were added at such a rate that the internal temperature of <37° C. could be maintained. After completion of the addition, the mixture was stirred for a further 1 h., then the precipitate was filtered off under suction, rinsed well with dichloromethane and the filtrate was evaporated. The residual yellow oil was subjected to chromatography on silica gel with hexane/ethyl acetate 50:50. There were obtained 15.66 g (92%) of 4-methyl-[1,2,3]thiadiazole-5-carboxylic acid phenethylamide as a colorless crystallizate of m.p. 64°-68° C. Recrystallization of a sample from tert.-butyl methyl ether gave colorless crystals of m.p. 64.5°-66° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05866583
出典データセットuspto-grants-1999_02
ORD IDord-eef205f0552743a184c7c6b5967655c8
出典メモuspto-grants-1999_02