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HRID 633671作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Ethyl bromoacetateHCID 7748—
反応物Potassium CarbonateHCID 11430—
反応物1-[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—
溶媒DimethylformamideHCID 6228—
生成物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]-xanthineHCID 66753750—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09321791B2
出典データセットuspto-grants-2016_04
ORD IDord-cf2f2c7489bf451d88afee5616a4cb14
出典メモuspto-grants-2016_04