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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39991생성일: 2026년 10월 24일

Sodium Bicarbonate → 1-(2-(4-((3-fluoro-4-methylbenzyl)amino)piperidin-1-yl)ethyl)-7-fluoroquinoxalin-2(1H)-one

https://huagongshe.com/ko/reaction/39991

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물3-Fluoro-4-methylbenzaldehydeHCID 2774574—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1-(2-(4-aminopiperidin-1-yl)ethyl)-7-fluoroquinoxalin-2(1H)-oneHCID 59397907—
용매Acetic AcidHCID 176—
용매ChloroformHCID 6212—
생성물1-(2-(4-((3-fluoro-4-methylbenzyl)amino)piperidin-1-yl)ethyl)-7-fluoroquinoxalin-2(1H)-oneHCID 1598563389.8%

반응 단계

To 10 mL of a chloroform solution containing 383 mg of 1-(2-(4-aminopiperidin-1-yl)ethyl)-7-fluoroquinoxalin-2(1H)-one and 160 mg of 3-fluoro-4-methylbenzaldehyde, 76 μL of acetic acid was added, and stirred at room temperature for 1 hour. To the reaction mixture, 437 mg of sodium triacetoxyborohydride was added, and stirred overnight. Aqueous saturated sodium hydrogen carbonate solution was added, 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; Fuji Silysia Chemical Ltd., Chromatorex-NH, eluent; ethyl acetate:hexane=1:1] to give 429 mg of 1-(2-(4-((3-fluoro-4-methylbenzyl)amino)piperidin-1-yl)ethyl)-7-fluoroquinoxalin-2(1H)-one as a pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524738B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-a9370aa48cd34bffa914da278f52abae
출처 메모uspto-grants-2013_09