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HRID 606957作成日:2026年10月25日
Methanesulfonyl chloride → N-[5-(5-Cyanopyridin-3-ylethynyl)-2-fluorophenyl]-N-methanesulfonyl-methanesulfonamide
https://huagongshe.com/reaction/606957
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | 5-(3-Amino-4-fluorophenylethynyl)-nicotinonitrile | HCID 67047822 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | N-[5-(5-Cyanopyridin-3-ylethynyl)-2-fluorophenyl]-N-methanesulfonyl-methanesulfonamide | HCID 67047709 | 36.2% |
反応手順
Dissolve 5-(3-amino-4-fluorophenylethynyl)-nicotinonitrile, (prepared as described in EXAMPLE 160), (0.2 g, 0.8 mmol) in anhydrous pyridine. Add a solution of methanesulfonyl chloride (0.2 g, 1.9 mmol) in tetrahydrofuran to the reaction and heat at 50° C. for 16 h. Concentrate and dissolve the crude reaction in ethyl acetate and water. Wash the organic layer with water, an aqueous saturated solution of sodium chloride, dry (potassium carbonate), filter, concentrate and purify (silica gel chromatography, eluting with 100:0 to 80:20 dichloromethane:ethyl acetate), to give the title compound as a white solid (114 mg, 36%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07915424B2 |
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| 出典データセット | uspto-grants-2011_03 |
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| ORD ID | ord-094567534f3147359f544421396bb3f5 |
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| 出典メモ | uspto-grants-2011_03 |
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