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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4835생성일: 2026년 10월 24일

Isopropanol → 2,3-Dihydro-4-methyl-2-[2-(4-morpholinyl)ethyl]-pyrido[3,2-f][1,4]oxazepin-5(4H)-one maleate

https://huagongshe.com/ko/reaction/4835

반응식

참여 물질

역할이름HCID투입량
반응물IsopropanolHCID 3776—
반응물MorpholineHCID 8083—
반응물Sodium HydroxideHCID 14798—
반응물Maleic AcidHCID 444266—
반응물2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]oxazepin-5(4H)one hydrochlorideHCID 13726437—
생성물2,3-Dihydro-4-methyl-2-[2-(4-morpholinyl)ethyl]-pyrido[3,2-f][1,4]oxazepin-5(4H)-one maleateHCID 13726489—

반응 단계

2-(2-Chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]oxazepin-5(4H)-one hydrochloride, 16 g (058 mole) was dissolved in morpholine (30 mL) and stirred overnight at room temperature. To the solution was added dilute sodium hydroxide solution (50 ml) and the resulting mixture extracted with chloroform (3×30 ml). The chloroform was removed on the rotary evaporator with aspiration. The residual morpholine was removed in vacuo at 50° C. (rotary evaporator). To the residual free base (15.5 g, 0.053 mole) was added isopropyl alcohol (1 liter) and maleic acid (9.24 g g, 0.080 mole). The mixture was heated to boiling and the clear solution cooled at 20° C. for several hours. The resulting crystals, 16 g (68.1%), were recrystallized from isopropyl alcohol, m.p. 163°-165° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04727152
출처 데이터셋uspto-grants-1988_02
ORD IDord-86d68c4097fe4b1490aca906d3daf585
출처 메모uspto-grants-1988_02