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HRID 407975作成日:2026年10月25日

Sodium Carbonate → (S)-3-((2,5-difluoro-4-(methylsulfonyl)phenyl)(methyl)amino)-1'-(5-ethylpyrimidin-2-yl)-1,4'-bipiperidin-2-one

https://huagongshe.com/reaction/407975

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物1,2,4-Trifluoro-5-(methylsulfonyl)benzeneHCID 46739396—
反応物(S)-1'-(5-ethylpyrimidin-2-yl)-3-(methylamino)-1,4'-bipiperidin-2-oneHCID 67470730—
溶媒DimethylformamideHCID 6228—
生成物(S)-3-((2,5-difluoro-4-(methylsulfonyl)phenyl)(methyl)amino)-1'-(5-ethylpyrimidin-2-yl)-1,4'-bipiperidin-2-oneHCID 8668811228%

反応条件

温度130 °C

反応手順

(S)-1′-(5-ethylpyrimidin-2-yl)-3-(methylamino)-1,4′-bipiperidin-2-one (0.040 g, 0.13 mmol), 1,2,4-trifluoro-5-(methylsulfonyl)benzene (Preparation C, 0.053 g, 0.25 mmol) and Na2CO3 (0.040 g, 0.38 mmol) were dissolved in DMF (1 mL) and heated at 130° C. overnight. The reaction was concentrated and the residue was purified using preparative TLC (100% EtOAc) to afford (S)-3-((2,5-difluoro-4-(methylsulfonyl)phenyl)(methyl)amino)-1′-(5-ethylpyrimidin-2-yl)-1,4′-bipiperidin-2-one (0.018 g, 0.035 mmol, 28% yield) as yellow solid. Mass spectrum (apci) m/z=508.3 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754226B2
出典データセットuspto-grants-2014_06
ORD IDord-e88004b53ccb4100a1ec2b880703e257
出典メモuspto-grants-2014_06