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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 395852생성일: 2026년 10월 24일

Toluene → N-(4-Methoxyphenyl)-2-[1-(4-pyridinyl)piperidin-4-yloxycarbonyl]aminobenzamide

https://huagongshe.com/ko/reaction/395852

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물PhosgeneHCID 6371—
반응물Methanesulfonic AcidHCID 6395—
반응물QuinolineHCID 7047—
반응물2-amino-N-(4-methoxyphenyl)benzamideHCID 478820—
반응물1-(Pyridin-4-yl)piperidin-4-olHCID 23447619—
용매DichloromethaneHCID 6344—
생성물N-(4-Methoxyphenyl)-2-[1-(4-pyridinyl)piperidin-4-yloxycarbonyl]aminobenzamideHCID 1817441846%

반응 단계

To a mixture of 1-(4-pyridyl)-4-hydroxypiperidine (536 mg, 3.01 mmol) and methylene chloride (45 mL) was added methanesulfonic acid (0.2 ml, 3.1 mmol). After stirring for 15 seconds, quinoline (0.45 mL, 3.8 mmol) was added, immediately followed by 1.93 M phosgene in toluene (2 mL, 3.9 mmol). After 5 minutes, the reaction was placed in a 35° C. oil bath for 45 minutes. The reaction was cooled to room temperature and N-(4-methoxyphenyl)-2-aminobenzamide (728 mg, 3.0 mmol) and quinoline(0.45 mL, 3.8 mmol) were added. After stirring overnight, the reaction was diluted with CH2Cl2(150 mL) and washed with sat'd sodium carbonate (2×25 mL). The organic layer was concentrated and the crude residue was chromatographed to give 617 mg (46%) of the title compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06605626B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-2df88400879e4876b1fd1e7676a166ee
출처 메모uspto-grants-2003_08