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HRID 1250976作成日:2026年10月27日

Potassium Carbonate → 3-(3-Aminopropyl)-2-thiazolidinone

https://huagongshe.com/reaction/1250976

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物18-Crown-6HCID 28557—
反応物2-ThiazolidinoneHCID 97431—
反応物Sodium borohydrideHCID 4311764—
反応物n-Phthalimido-3-bromopropylamineHCID 22597359—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒IsopropanolHCID 3776—
溶媒AcetonitrileHCID 6342—
生成物3-(3-Aminopropyl)-2-thiazolidinoneHCID 1013010255%

反応条件

温度60 °C

反応手順

To a solution of 2-thiazolidinone (0.994 g, 9.64 mmol) in acetonitrile (10 ml) were added N-phthalimido-3-bromopropylamine (2.88 g, 10.7 mmol), potassium carbonate (1.64 g, 11.9 mmol), and 18-crown-6 (catalytic amount). The mixture was refluxed about 17 hours, solvent was removed in vacuo, and the resulting solid was redissolved in 1 M potassium chloride and dichioromethane (˜25 ml each). The aqueous phase was separated and extracted with 2×25 ml dichloromethane. The combined organic fraction was dried over sodium sulfate, filtered and dried in vacuo. The crude product was recrystallized from acetone/methanol to give 1.54 g (55% yield). To a warmed solution of the phthalimido protected amine (1.53 g, 5.27 mmol) in 6:1 isopropanol:water was added sodium borohydride (1.01 g, 26.7 mmol), and the mixture was stirred at 60° C. for 22 hours. Glacial acetic acid (5.4 ml) was added, and the solution was stirred at 80° C. for 2 hours, then the solution was cooled and dried in vacuo. The product was redissolved in 6 N hydrochloric acid, washed with ether (2×30 ml), then dried in vacuo. The product was purified via recrystallization from hot water.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06340746B1
出典データセットuspto-grants-2002_01
ORD IDord-6da9c28a19664bfeac740e7682ca8d60
出典メモuspto-grants-2002_01