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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1193850생성일: 2026년 10월 27일

Diethylamine → 7-Chloro-2-[2-(diethylamino)ethyl]-2,3-dihydro-4-methylpyrido[3,2-f][1,4]-oxazepin-5(4H)-one oxalate

https://huagongshe.com/reaction/1193850

반응식

참여 물질

역할이름HCID투입량
반응물DiethylamineHCID 8021—
반응물Ammonium HydroxideHCID 14923—
반응물7-Chloro-2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]oxazepin-5(4H)-oneHCID 13726445—
반응물Ethylacetate methanolHCID 21584119—
용매EthanolHCID 702—
생성물7-Chloro-2-[2-(diethylamino)ethyl]-2,3-dihydro-4-methylpyrido[3,2-f][1,4]-oxazepin-5(4H)-one oxalateHCID 1372659876%

반응 단계

To a suspension of 7-chloro-2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]oxazepine-5(4H)-one in 50 ml of absolute ethanol was added 2.26 ml (0.022 mole) of diethylamine and the mixture heated to reflux. (Complete dissolution occurred). After 1 hr, another 2.26 ml (0.022 mole) of diethylamine was added followed by 5.0 ml (0.049 mole) and heating continued for 2 more hours. TLC (ethylacetate/methanol/conc. ammonium hydroxide, 7:2:1, v/v/v) still showed presence of starting material; another 2.26 ml (0.022 mole) of diethylamine was added and heating continued for 15 hr at reflux. Solvent was removed by rotary evaporation (60° C., 30 mm Hg) and the residue taken up in methylene chloride, washed twice with dilute aqueous sodium hydroxide and once with water. The organic layer was dried over sodium sulfate, filtered and concentrated by rotary evaporation, and azeotroped once with toluene. The oil was treated with oxalic acid in isopropyl alcohol which yielded 6.7 g (76%) of white crystals, m.p. 163°-164° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04810795
출처 데이터셋uspto-grants-1989_03
ORD IDord-4005129756644a39acf3a294a465b06f
출처 메모uspto-grants-1989_03