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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4861생성일: 2026년 10월 23일

Dimethyl Sulfoxide → 2-[2-(1-Azetidinyl)ethyl]-2,3-dihydro-4-methylpyrido[3,2-f][1,4]oxazepine-5(4H)-thione fumarate

https://huagongshe.com/ko/reaction/4861

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물AzetidineHCID 10422—
반응물Potassium CarbonateHCID 11430—
반응물2-(chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f]-1,4-oxazepine-5(4H)thioneHCID 13726442—
생성물2-[2-(1-Azetidinyl)ethyl]-2,3-dihydro-4-methylpyrido[3,2-f][1,4]oxazepine-5(4H)-thione fumarateHCID 1372656231%

반응 단계

To 5.0 g (0.0914 mole) of 2-(2-chloroethyl)-2,5-dihydro-4-methylpyrido[3,2-f]-1,4-oxazepine-5(4H)-thione dissolved in 50 ml of dimethylsulfoxide was added 8.04 g (0.058 mole) of potassium carbonate and 1.21 g (0.021 mole) of azetidine. The reaction mixture was stirred at room temperature for 8 hr after which was added 0.5 g (0.009 mole) of azetidine and the mixture was stirred overnight at room temperature. An additional 0.3 g (0.005 mole of azetidine was added and stirring was continued for 24 hr. The mixture was filtered and solvent removed by rotary evaporator at 80° C., 0.5 mm Hg. The residue was taken up in 100 ml of chloroform and the solution was washed with two 30 ml portions of dilute aqueous sodium hydroxide. The organic layer was dried over magnesium sulfate, filtered and concentrated by rotary evaporator. The residue was reacted with fumaric acid in isopropyl alcohol to give 2.5 g (31%) of pale yellow crystals, m.p. 122°-126° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04727152
출처 데이터셋uspto-grants-1988_02
ORD IDord-cad802f8607b497e826f6484b8b5dd8e
출처 메모uspto-grants-1988_02