돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1043030생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1043030

반응식

참여 물질

역할이름HCID투입량
반응물2-(4-Chlorophenoxy)anilineHCID 76010—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1-acetyl-N-(2-acetylphenyl)piperidine-4-carboxamideHCID 17145786—
촉매Acetic AcidHCID 176—
촉매Chlorotitanium triisopropoxideHCID 3084342—
용매DichloromethaneHCID 6344—
생성물1-Acetyl-N-(2-(1-(2-(4-chlorophenoxy)phenylamino)ethyl)phenyl)piperidine-4-carboxamideHCID 4261360310%

반응 단계

2-(4-Chlorophenoxy)aniline (25 mg, 0.1138 mmol, 1.1 eq) and 1-acetyl-N-(2-acetylphenyl)piperidine-4-carboxamide (30 mg, 0.1040 mmol, 1 eq) were stirred in dry dichloromethane (DCM) at room temperature for 10 min. Tri-isopropoxytitanium chloride (55 μL, 0.2303 mmol, 2.2 eq) was added to the reaction mixture which was stirred at room temperature for an additional 10 min. Sodium triacetoxyborohydride (110 mg, 0.5190 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 (50 mL) and extracted with DCM (30 mL). The organic layer was washed with brine (50 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 (5 mg, 10%) as a clear oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08558028B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-9efb7f91417d4f318acce73adabc7f10
출처 메모uspto-grants-2013_10