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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1727345생성일: 2026년 10월 26일

Water → 1-(4-Methoxyphenyl)-2-(2-tert-butoxycarbonylamino-4-pyridyl)ethanone

https://huagongshe.com/reaction/1727345

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Diisopropyl EtherHCID 7914—
반응물tert-butyl N-(4-methylpyridin-2-yl)carbamateHCID 11063648—
반응물HCID 178418244HCID 178418244—
용매TetrahydrofuranHCID 8028—
생성물1-(4-Methoxyphenyl)-2-(2-tert-butoxycarbonylamino-4-pyridyl)ethanoneHCID 1161709269%

반응 조건

온도-78 °C

반응 단계

A solution of 2-tert-butoxycarbonylamino-4-methylpyridine (20 g, 97 mmol) in anhydrous tetrahydrofuran (300 mL) was cooled to −78° C., and to this was added dropwise a 1.6 M n-butyllithium hexane solution (140 mL, 0.23 mol) with stirring. After completion of the addition, the solution was stirred for 30 minutes at 0° C., then, the solution was cooled to −78° C. A solution of N-(4-methoxybenzoyl)propyleneimine (25 g, 0.13 mol) in anhydrous tetrahydrofuran (50 mL) was added dropwise. After completion of the addition, the reaction mixture was stirred for 2 hours at room temperature. To the reaction mixture was added water (100 mL) and isopropyl ether (300 mL), and the resulted crude crystal was filtrated. This crude crystal was recrystallized from tetrahydrofuran-hexane to obtain a title compound (23 g, yield: 69%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07495018B2
출처 데이터셋uspto-grants-2009_02
ORD IDord-ed1d5cbfb8bd42cba4379ff97c1d26a6
출처 메모uspto-grants-2009_02