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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 633671생성일: 2026년 10월 25일

Water → 1-(2-{2-[(Ethoxycarbonyl)methoxy]-phenyl}-2-oxo-ethyl)-3-methyl-7-(3-methyl-2-buten-1-yl)-8-[3-(tert.-butyloxycarbonylamino)-piperidin-1-yl]-xanthine

https://huagongshe.com/reaction/633671

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Ethyl bromoacetateHCID 7748—
반응물Potassium CarbonateHCID 11430—
반응물1-[2-(2-Hydroxy-phenyl)-2-oxo-ethyl]-3-methyl-7-(3-methyl-2-buten-1-yl)-8-[3-(tert.-butyloxycarbonylamino)-piperidin-1-yl]-xanthineHCID 66723736—
용매DimethylformamideHCID 6228—
생성물1-(2-{2-[(Ethoxycarbonyl)methoxy]-phenyl}-2-oxo-ethyl)-3-methyl-7-(3-methyl-2-buten-1-yl)-8-[3-(tert.-butyloxycarbonylamino)-piperidin-1-yl]-xanthineHCID 66753750—

반응 단계

63 mg of ethyl bromoacetate are added to a mixture of 200 mg of 1-[2-(2-hydroxy-phenyl)-2-oxo-ethyl]-3-methyl-7-(3-methyl-2-buten-1-yl)-8-[3-(tert.-butyloxycarbonylamino)-piperidin-1-yl]-xanthine and 63 mg of potassium carbonate in 3 ml N,N-dimethylformamide. The reaction mixture is stirred for five hours at ambient temperature. For working up it is combined with water and the precipitate formed is suction filtered, washed with water and dried for three hours at 80° C. in the drying cupboard.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09321791B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-cf2f2c7489bf451d88afee5616a4cb14
출처 메모uspto-grants-2016_04