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HRID 248832作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物2-FuranmethanethiolHCID 7363—
反応物PiperidineHCID 8082—
反応物Benzyltrimethylammonium hydroxideHCID 66854—
反応物8-chloro-N-(2-oxo-3-butenyl)dibenz-[b,f][1,4]oxazepin-10(11H)-carboxamideHCID 10831197—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物8-chloro-N-[4-[(2-furanylmethyl)thio]-2-oxobutyl]dibenz[b,f][1,4]oxazepin-10(11H)-carboxamideHCID 10742479—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05212169
出典データセットuspto-grants-1993_05
ORD IDord-4f1d21f2d9974500b6b242551c69a2b2
出典メモuspto-grants-1993_05