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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 248832생성일: 2026년 10월 26일

2-Furanmethanethiol → 8-chloro-N-[4-[(2-furanylmethyl)thio]-2-oxobutyl]dibenz[b,f][1,4]oxazepin-10(11H)-carboxamide

https://huagongshe.com/reaction/248832

반응식

참여 물질

역할이름HCID투입량
반응물2-FuranmethanethiolHCID 7363—
반응물PiperidineHCID 8082—
반응물Benzyltrimethylammonium hydroxideHCID 66854—
반응물8-chloro-N-(2-oxo-3-butenyl)dibenz-[b,f][1,4]oxazepin-10(11H)-carboxamideHCID 10831197—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물8-chloro-N-[4-[(2-furanylmethyl)thio]-2-oxobutyl]dibenz[b,f][1,4]oxazepin-10(11H)-carboxamideHCID 10742479—

반응 단계

A solution of 8-chloro-N-(2-oxo-3-butenyl)dibenz[b,f][1,4]oxazepin-10(11H)-carboxamide (0.75 gram), furfuryl mercaptan (0.23 mL), piperidine (0.069 mL), and N-benzyltrimethylammonium hydroxide (0.069 mL) in methylene chloride (12 mL) and methanol (3 mL) was stirred at room temperature for 6 hours. The reaction was diluted with methylene chloride (75 mL), washed with 75 mL each of 1N HCl (two times), water, saturated aqueous sodium bicarbonate, and brine, dried over MgSO4, and evaporated in vacuo. The crude product was purified by flash chromatography through silica gel 60 (350 mL) using 95:5 methylene chloride: ethyl acetate to yield a colorless oil. Analysis calculated for C23H21ClN2O4S×0.1 EtOAc: C, 60.34; H, 4.72; N, 6.01; Cl, 7.61; S, 6.88. Found: C, 59.94; H, 4.84; N, 5.87; Cl, 8.13; S, 6.65.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05212169
출처 데이터셋uspto-grants-1993_05
ORD IDord-4f1d21f2d9974500b6b242551c69a2b2
출처 메모uspto-grants-1993_05