돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1943687생성일: 2026년 10월 27일

Water → (2,3-Dihydro-pyrido[4,3-b][1,4]oxazin-4-yl)-(3-methoxy-isoxazol-5-yl)-methanone

https://huagongshe.com/reaction/1943687

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriethylamineHCID 8471—
반응물3-Methoxy-5-isoxazolecarbonyl chlorideHCID 12196359—
반응물2H,3H,4H-pyrido[4,3-b][1,4]oxazineHCID 21885950—
용매DichloromethaneHCID 6344—
생성물(2,3-Dihydro-pyrido[4,3-b][1,4]oxazin-4-yl)-(3-methoxy-isoxazol-5-yl)-methanoneHCID 44608544—

반응 단계

In a 10 ml flask, 3,4-dihydro-2H-pyrido[4,3-b][1,4]oxazine (100 mg, 0.73 mmol) and 3-methoxy-isoxazol-5-carbonyl chloride (131 mg, 0.80 mmol) were dissolved in dichloromethane. Triethylamine (0.51 ml, 3.65 mmol) was added thereto and then stirred at room temperature for 2 hours. After completion of the reaction by adding water dropwise, the reaction mixture was extracted with dichloromethane, and the combined organic layer was dried over anhydrous sodium sulfate (Na2SO4), filtered and evaporated under reduced pressure. The residue was purified by column chromatography on amine silica eluting with a solvent of dichloromethane:methanol=30:1. The fractions containing the product were collected and evaporated to obtain the target compound 43, i.e., (2,3-dihydro-pyrido[4,3-b][1,4]oxazin-4-yl)-(3-methoxy-isoxazol-5-yl)-methanone, as pale-brown solid (149 mg, 78%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08394792B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-bf094ab021954322a9bee2d356e54902
출처 메모uspto-grants-2013_03