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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1043031생성일: 2026년 10월 26일

2-(4-Chlorophenoxy)aniline → 1-Acetyl-N-(3-(1-(2-(4-chlorophenoxy)phenylamino)ethyl)phenyl)piperidine-4-carboxamide

https://huagongshe.com/reaction/1043031

반응식

참여 물질

역할이름HCID투입량
반응물2-(4-Chlorophenoxy)anilineHCID 76010—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1-acetyl-N-(3-acetylphenyl)piperidine-4-carboxamideHCID 40218423—
촉매Acetic AcidHCID 176—
촉매Chlorotitanium triisopropoxideHCID 3084342—
용매DichloromethaneHCID 6344—
생성물1-Acetyl-N-(3-(1-(2-(4-chlorophenoxy)phenylamino)ethyl)phenyl)piperidine-4-carboxamideHCID 5957167818%

반응 단계

2-(4-Chlorophenoxy)aniline (137 mg, 0.6237 mmol, 1.1 eq) and 1-acetyl-N-(3-acetylphenyl)piperidine-4-carboxamide (160 mg, 0.5549 mmol, 1 eq) were stirred in dry dichloromethane (DCM) at room temperature for 10 min. Tri-isopropoxytitanium chloride (295 μL, 1.2351 mmol, 2.2 eq) was added to the reaction mixture which was stirred at room temperature for an additional 10 min. Sodium triacetoxyborohydride (590 mg, 2.7838 mmol, 5 eq) and acetic acid (3 drops) were added to the reaction mixture which was stirred at room temperature for 16 h. The reaction mixture was then poured onto a solution of saturated aqueous sodium bicarbonate (100 mL) and extracted with DCM (80 mL). The organic layer was washed with brine (100 mL), dried over MgSO4, filtered and concentrated to give the crude as a yellow oil. Purification of the crude by flash chromatography (ISCO) eluting with a gradient [from 100% petroleum ether (PE) to 100% EtOAc] gave the title compound (48 mg, 18%) as a clear oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08558028B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-3070a69fa6bc4992aa570315dc4b501b
출처 메모uspto-grants-2013_10