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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1676525생성일: 2026년 10월 26일

Triethylamine → 4-amino-N-(1-ethyl-piperidin-4-yl)-benzamide

https://huagongshe.com/reaction/1676525

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-Ethylpiperidin-4-amineHCID 3734990—
반응물4-Amino-benzoic acid benzotriazol-1-yl esterHCID 53844583—
용매TetrahydrofuranHCID 8028—
생성물4-amino-N-(1-ethyl-piperidin-4-yl)-benzamideHCID 5491589584%

반응 단계

To a mixture of 1.0424 g (4.1 mmole) of 4-amino-benzoic acid benzotriazol-1-yl ester and 8 mL of dry tetrahydrofuran at 0 degrees was added 0.5257 g (4.1 mmole) of 4-amino-1-ethylpiperidine followed by 1.0372 g (10.3 mmole) of triethylamine. The cooling bath was removed and the mixture stirred at room temperature for 65 minutes. Volatiles were removed under reduced pressure and the residue taken up in ethyl acetate, and the organic layer washed twice with 50 mL of 0.5 M sodium carbonate, 50 mL water, and then 50 mL brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 0.8522 g 4-amino-N-(1-ethyl-piperidin-4-yl)-benzamide, as a white solid which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08003785B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-6618e55103764c5285ec53a92e237d85
출처 메모uspto-grants-2011_08