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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 233474생성일: 2026년 10월 25일

Dicyclohexylcarbodiimide → N,N-Dimethylaniline

https://huagongshe.com/reaction/233474

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물(alphaZ)-2-Amino-alpha-(methoxyimino)-4-thiazoleacetic acidHCID 5486924—
용매DimethylformamideHCID 6228—
생성물N,N-DimethylanilineHCID 949254%

반응 단계

A mixture of 1.00 g (5.00 mmol) of (Z)-2-(2-aminothiazol-4-yl)-2-methoxyiminoacetic acid, 0.76 g (5.00 mmol) of 1-hydroxy-1H-benzotriazole hydrate, 1.14 g (5.50 mmol) of dicyclohexylcarbodiimide and 20 ml of N,N-dimethylformamide was stirred at room temperature for 2 hours. The obtained white solid was filtered and the filtrate was cooled to 0° C. The filtrate was added to mixed solution of 2.5 g (5.00 mmol) of 7-amino-3-(2,3-cyclopenteno-4-carbamoyl-1-pyridinium)methyl-3-cephem-4-carboxylate hydroiodic acid obtained in Preparation Example 24, 10 ml of N,N-dimethylformamide and 1.6 ml (12.70 mmol) of N,N-dimethylaniline. The mixture was stored at room temperature overnight and the precipitate was removed therefrom. The residue was dropped into 500 ml of diethylether with stirring. The precipitate was filtered, triturated with 100 ml of acetone and filtered again. The crude product thus obtained was dissolved in 100 ml of water and insoluble material was discarded by filtration. The resultant was freeze-dried to obtain 1.0 g of the same compound as obtained in Method a (yield: 37%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05593985
출처 데이터셋uspto-grants-1997_01
ORD IDord-5d3092061b6447a4894af552dc3e80fb
출처 메모uspto-grants-1997_01