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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 704445생성일: 2026년 10월 24일

Dicyclohexylcarbodiimide → 1-(3-Methyl-3-phenylbutyl)-4-[2-(3-pyridyl)thiazolidin-4-ylcarbonyl]piperazine

https://huagongshe.com/ko/reaction/704445

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물2-(3-Piridyl)thiazolidine-4-carboxylic acidHCID 327593—
반응물1-(3-Methyl-3-phenylbutyl)piperazineHCID 14649430—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물1-(3-Methyl-3-phenylbutyl)-4-[2-(3-pyridyl)thiazolidin-4-ylcarbonyl]piperazineHCID 13143699%

반응 단계

A solution of 2-(3-pyridyl)thiazolidin-4-carboxylic acid (0.81 g), 1-(3-methyl-3-phenylbutyl)-piperazine (0.73 g), 1-hydroxybenzotriazole (0.50 g) and dicyclohexylcarbodiimide (0.76 g) in N,N-dimethylformamide (7 ml) was stirred under room temperature for 12 hours. To the reaction solution was added ethyl acetate (10 ml) and the insoluble matter was filtered off. To the filtrate was added 0.5N sodium hydroxide and the solution was extracted with ethyl acetate. The ethyl acetate layer was extracted with 1N hydrochloric acid. The aqueous layer was made basic with potassium carbonate and extracted with ethyl acetate. The resultant ethyl acetate layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography and elution with an ethyl acetate-methanol (10:1) mixture gave 1.32 g of 1-(3-methyl-3-phenylbutyl)-4-[2-(3-pyridyl)thiazolidin-4-ylcarbonyl]piperazine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04987132
출처 데이터셋uspto-grants-1991_01
ORD IDord-0d3b88db7f154e0987b374ea4a659f80
출처 메모uspto-grants-1991_01