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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 1,2,4-Trifluoro-5-(methylsulfonyl)benzene | HCID 46739396 | — |
| 反応物 | (S)-1'-(5-ethylpyrimidin-2-yl)-3-(methylamino)-1,4'-bipiperidin-2-one | HCID 67470730 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | (S)-3-((2,5-difluoro-4-(methylsulfonyl)phenyl)(methyl)amino)-1'-(5-ethylpyrimidin-2-yl)-1,4'-bipiperidin-2-one | HCID 86688112 | 28% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08754226B2 |
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| 出典データセット | uspto-grants-2014_06 |
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| ORD ID | ord-e88004b53ccb4100a1ec2b880703e257 |
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| 出典メモ | uspto-grants-2014_06 |
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