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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1291106생성일: 2026년 10월 27일

2-Dimethylaminopyridine → 1-Benzyl-piperidin-4-yl 2-dimethylamino-benzoate

https://huagongshe.com/reaction/1291106

반응식

참여 물질

역할이름HCID투입량
반응물2-DimethylaminopyridineHCID 21885—
반응물2-(Dimethylamino)benzoic acidHCID 69118—
반응물1-Benzylpiperidin-4-olHCID 78461—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매DimethylformamideHCID 6228—
생성물1-Benzyl-piperidin-4-yl 2-dimethylamino-benzoateHCID 1891977646%

반응 단계

0.33 g (0.002 mol) of 2-dimethylaminobenzoic acid was dissolved in 10 ml of dimethylformamide, treated with 0.122 g (0.001 mol) of dimethylaminopyridine and 0.383 g (0.002 mol) of 1-benzyl-4-hydroxypiperidine and cooled to 0°. 0.422 g (0.0022 mol) of N-ethyl-N'-(3-dimethylaminopropyl)-carbodiimide hydrochloride was added and the mixture was stirred at 0° for a further 2 hrs. Subsequently, the mixture was stirred at room temperature for 3 days, the solvent was distilled off and the residue was chromatographed on silica gel with ethyl acetate/hexane (1:2). 0.31 g (46%) of 1-benzyl-piperidin-4-yl 2-dimethylamino-benzoate was obtained as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05753679
출처 데이터셋uspto-grants-1998_05
ORD IDord-79eaf0e3929f46ba9c6fd28300d0b724
출처 메모uspto-grants-1998_05