戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 54079作成日:2026年10月26日

Tert-Butylamine → 3-(benzyloxycarbonyl)-N-tert.butyl-4(R)-thiazolidinecarboxamide

https://huagongshe.com/reaction/54079

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-ButylamineHCID 6385—
反応物EthylmorpholineHCID 7525—
反応物Isobutyl chloroformateHCID 62365—
反応物(R)-3-((Benzyloxy)carbonyl)thiazolidine-4-carboxylic acidHCID 11119045—
溶媒TetrahydrofuranHCID 8028—
生成物3-(benzyloxycarbonyl)-N-tert.butyl-4(R)-thiazolidinecarboxamideHCID 1864827388.6%

反応条件

温度-15 °C

反応手順

A solution of 2.67 g of N-benzyloxycarbonyl-4(R)-thiazolidinecarboxylic acid in 42 ml of dry tetrahydrofuran was stirred and cooled to -15° C. in an ice/salt bath while there were added 1.15 g of N-ethylmorpholine followed after 2 minutes by 1.87 g of isobutyl chloroformate. After a further 3 minutes 0.73 g of tert.butylamine was added dropwise and the mixture was then allowed to warm to room temperature and was stirred overnight. Tetrahydrofuran was removed by evaporation under reduced pressure and the residue was dissolved in dichloromethane. The solution was washed in sequence with water, 10% citric acid solution, water, saturated sodium bicarbonate solution and water, then dried over anhydrous sodium sulphate, filtered and evaporated to give 2.85 g of 3-(benzyloxycarbonyl)-N-tert.butyl-4(R)-thiazolidinecarboxamide as a solid which melted at 96°-98° C. after recrystallization from diethyl ether/n-hexane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05620987
出典データセットuspto-grants-1997_04
ORD IDord-1f89d22ddfca4c4eb98f2b8f40ae0506
出典メモuspto-grants-1997_04