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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13864생성일: 2026년 10월 24일

1,2-Dichloroethane → N-{2-[4-(Biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]ethyl}-3-methoxy-N-methylterephthalamic Acid Methyl Ester

https://huagongshe.com/ko/reaction/13864

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물DiisopropylethylamineHCID 81531—
반응물HOAtHCID 181649—
반응물1-(2-(Methylamino)ethyl)piperidin-4-yl [1,1'-biphenyl]-2-ylcarbamateHCID 56643603—
반응물2-Methoxy-4-(methoxycarbonyl)benzoic acidHCID 59340334—
용매DimethylformamideHCID 6228—
생성물N-{2-[4-(Biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]ethyl}-3-methoxy-N-methylterephthalamic Acid Methyl EsterHCID 5934033289%

반응 단계

To a stirred solution of 2-methoxyterephthalic acid 4-methyl ester (450 mg, 2.1 mmol; prepared as described in Preparation 18) in DMF (10 mL) was added EDC (630 mg, 3.3 mmol), HOAt (2.4 mL, 1.18 mmol, 0.5M in DMF) and DIPEA (1.3 mL, 7.05 mmol). When the mixture was homogenous, a solution of biphenyl-2-ylcarbamic acid 1-(2-methylaminoethyl)piperidin-4-yl ester (830 mg, 2.4 mmol; prepared as described in Preparation 4) was added slowly. The reaction mixture was stirred at room temperature for 16 hours and then washed with water (100 mL), 1N HCl (100 mL), 1N NaOH (100 mL), brine (100 mL), dried over MgSO4, filtered and concentrated to afford the title intermediate in 89% yield (1.04 g, 1.9 mmol). MS m/z: [M+H+] calcd for C31H35N3O6, 545.6; found, 546.6.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728144B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-c96354509dec4955bc0831af79a7db73
출처 메모uspto-grants-2010_06