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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1177775생성일: 2026년 10월 26일

Triethylamine → N-(1-benzyl-piperidin-4-yl)-2-methoxy-6-nitrobenzamide

https://huagongshe.com/reaction/1177775

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1-Benzyl-4-piperidylamineHCID 415852—
반응물2-Methoxy-6-nitrobenzoic acidHCID 13300035—
용매Ethyl AcetateHCID 8857—
생성물N-(1-benzyl-piperidin-4-yl)-2-methoxy-6-nitrobenzamideHCID 2110222386%

반응 조건

온도40 °C

반응 단계

2-Methoxy-6-nitro-benzoic acid (2.0 g, 10.1 mmol), 4-amino-1-benzylpiperidine (1.9 mL, 10.1 mmol), 1-hydroxybenzotriazole (1.43 g, 10.5 mmol) and 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide (1.9 g, 10.1 mmol) were combined in ethyl acetate (25 mL). To this solution was added triethylamine (4.2 mL. 30.3 mmol) and the reaction mixture stirred at 40° C. for 2 h. After cooling to room temperature, the mixture was diluted with ethyl acetate and washed with water (2×), 5% sodium bicarbonate, brine (2×), dried over sodium sulfate, and concentrated to afford 3.2 g (86%) of the desired product. LC/MS: tR=1.10 min, 370.28 (MH)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07842808B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-2b74055737bb4bd19eff0b79415b2945
출처 메모uspto-grants-2010_11