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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2193357생성일: 2026년 10월 26일

Sodium Bicarbonate → 7-methoxy-1-(2-(4-((5-(thiophen-2-yl)isoxazol-3-yl)methylamino)piperidin-1-yl)ethyl)quinoxalin-2(1H)-one

https://huagongshe.com/reaction/2193357

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물5-Thiophen-2-yl-isoxazole-3-carbaldehydeHCID 2776546—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1-[2-(4-Aminopiperidin-1-yl)ethyl]-7-methoxyquinoxalin-2(1H)-oneHCID 59397838—
용매Acetic AcidHCID 176—
용매ChloroformHCID 6212—
생성물7-methoxy-1-(2-(4-((5-(thiophen-2-yl)isoxazol-3-yl)methylamino)piperidin-1-yl)ethyl)quinoxalin-2(1H)-oneHCID 5939835190.8%

반응 단계

To 10 mL of a chloroform solution containing 500 mg of 1-(2-(4-aminopiperidin-1-yl)ethyl)-7-methoxyquinoxalin-2(1H)-one and 267 mg of 5-(2-thienyl)-3-isoxazolecarbaldehyde, 100 mg of acetic acid was added, and stirred at room temperature for 2 hours. To the reaction mixture, 526 mg of sodium triacetoxyborohydride was added, and stirred for 18 hours. Aqueous saturated sodium hydrogen carbonate solution was added, and the organic layer was separated. The organic layer was washed with aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [Silica Gel; Kanto Chemical Co., Inc., Silica Gel 60N, eluent; chloroform:methanol=10:1], to give 0.63 g of 7-methoxy-1-(2-(4-((5-(thiophen-2-yl)isoxazol-3-yl)methylamino)piperidin-1-yl)ethyl)quinoxalin-2(1H)-one as a brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08329694B2
출처 데이터셋uspto-grants-2012_12
ORD IDord-89720e217edb4d74aa62a1fe03c55c54
출처 메모uspto-grants-2012_12