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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 842389생성일: 2026년 10월 25일

Phosgene → 5-(tert-butyldimethylsilyloxy)-2-phthalimido-N-[[1-(4-pyridyl)piperidin-4-yl]methoxycarbonyl]aniline

https://huagongshe.com/reaction/842389

반응식

참여 물질

역할이름HCID투입량
반응물PhosgeneHCID 6371—
반응물(1-(Pyridin-4-YL)piperidin-4-YL)methanolHCID 11310048—
반응물5-(Tert-butyldimethylsilyloxy)-2-phthalimidoanilineHCID 18174494—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
용매HexaneHCID 8058—
생성물5-(tert-butyldimethylsilyloxy)-2-phthalimido-N-[[1-(4-pyridyl)piperidin-4-yl]methoxycarbonyl]anilineHCID 1817452990%

반응 단계

A solution of 5-(tert-butyldimethylsilyloxy)-2-phthalimidoaniline (1.02 g, 2.77 mmol) in toluene (15 mL) was treated with a solution of 20% phosgene in toluene (2 mL) at reflux for 20 min. The volatile materials were removed in vacuo to give a tan solid, which was dissolved in dry methylene chloride (20 mL) and treated with 1-(4-pyridyl)piperidine-4-methanol (0.53 g, 2.77 mmol). The resulting suspension was stirred for 90 min then diluted with hexane. The mixture was allowed to stand overnight and the resulting precipitate collected by vacuum filtration and dried to yield 1.46 g (90%) of the title compound as a tan powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06372759B1
출처 데이터셋uspto-grants-2002_04
ORD IDord-0acbb8ff5c624ef08e87a912bafd0b0a
출처 메모uspto-grants-2002_04