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HRID 525076作成日:2026年10月25日

Potassium Carbonate → 4-N-[5-bromothieno[2,3-d]pyrimidin-4-yl]-1-N,1-N-dimethylcyclohexane-1,4-diamine

https://huagongshe.com/reaction/525076

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N,N-Dimethyl-1,4-cyclohexanediamineHCID 345823—
反応物5-Bromo-4-chlorothieno[2,3-d]pyrimidineHCID 45480299—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物4-N-[5-bromothieno[2,3-d]pyrimidin-4-yl]-1-N,1-N-dimethylcyclohexane-1,4-diamineHCID 68115342—

反応手順

A 50-mL round-bottom flask was charged with commercially available 5-bromo-4-chlorothieno[2,3-d]pyrimidine (300 mg, 1.20 mmol, 1.00 equiv), 1-N,1-N-dimethylcyclohexane-1,4-diamine (205 mg, 1.44 mmol, 1.20 equiv), potassium carbonate (497 mg, 3.60 mmol, 3.00 equiv) in N,N-dimethylformamide (10 mL). The resulting solution was stirred overnight at room temperature. The resulting solution was diluted with 100 mL of water. The resulting solution was extracted with 3×100 mL of ethyl acetate and the organic layers combined. The resulting mixture was washed with 3×200 mL of brine. The mixture was dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 250 mg (59%) of 4-N-[5-bromothieno[2,3-d]pyrimidin-4-yl]-1-N,1-N-dimethylcyclohexane-1,4-diamine as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09340554B2
出典データセットuspto-grants-2016_05
ORD IDord-0ac49c92bb634744a379bcff88c90d49
出典メモuspto-grants-2016_05