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HRID 527775作成日:2026年10月25日

Potassium Carbonate → N2-Butyl-9-(4-chlorobutyl)-8-(methyloxy)-9H-purine-2,6-diamine

https://huagongshe.com/reaction/527775

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物1-Bromo-4-chlorobutaneHCID 81364—
反応物HCID 178448879HCID 178448879—
溶媒DimethylformamideHCID 6228—
生成物N2-Butyl-9-(4-chlorobutyl)-8-(methyloxy)-9H-purine-2,6-diamineHCID 59252596109.4%

反応条件

温度50 °C

反応手順

N2-Butyl-8-(methyloxy)-9H-purine-2,6-diamine trifluoroacetate (5 g, 14.27 mmol) and potassium carbonate (4.93 g, 35.7 mmol) were suspended in DMF (40 ml) and heated to 50° C. under nitrogen for 30 mins. The mixture was cooled to room temperature, 1-bromo-4-chlorobutane (1.645 ml, 14.27 mmol) was added and stirring was continued at room temperature for 20 hours. The solvent was concentrated under vacuum and the residue was partitioned between DCM (100 ml) and water (100 ml). The layers were separated using a hydrophobic frit and the aqueous phase was re-extracted with DCM (100 ml). The combined organics extracts were concentrated in vacuo and the residue purified by chromatography using a FlashMaster apparatus (100 g silica cartridge) and using a DCM:methanol 0-25% gradient over 40 mins. The desired fractions were combined and concentrated under vacuum to give the impure title compound as a yellow oil (5.1 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09346806B2
出典データセットuspto-grants-2016_05
ORD IDord-fe90c88eedb1460a9ec0ed8c9c1d935a
出典メモuspto-grants-2016_05