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HRID 64258作成日:2026年10月24日
N-{3-[(2E)-3-(dimethylamino)prop-2-enoyl]phenyl}acetamide → N-(3-(3-cyano-2-(4-phenoxyphenyl)pyrazolo[1,5-a]pyrimidin-7-yl)phenyl)acetamide
https://huagongshe.com/ja/reaction/64258
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | N-{3-[(2E)-3-(dimethylamino)prop-2-enoyl]phenyl}acetamide | HCID 11183866 | — |
| 反応物 | HCID 178509389 | HCID 178509389 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | N-(3-(3-cyano-2-(4-phenoxyphenyl)pyrazolo[1,5-a]pyrimidin-7-yl)phenyl)acetamide | HCID 117668104 | 90% |
反応手順
To a solution of (E)-N-(3-(3-(dimethylamino)acryloyl)phenyl)acetamide (46 mg, 0.2 mmol) in HOAc (5 mL) was added 5-amino-3-(4-phenoxyphenyl)-1H-pyrazole-4-carbonitrile (55 mg, 0.2 mmol). The mixture was stirred at 118° C. for 4 hr. Then the reaction mixture was concentrated to a residue and partitioned between ethyl acetate (100 mL) and brine (100 mL). Organic layer was separated, washed with brine (2×100 mL), dried over sodium sulfate and concentrated to afford 80 mg (90%) of N-(3-(3-cyano-2-(4-phenoxyphenyl)pyrazolo[1,5-a]pyrimidin-7-yl)phenyl)acetamide as a colorless oil. MS (ESI) m/e [M+1]+ 446.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09447106B2 |
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| 出典データセット | uspto-grants-2016_09 |
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| ORD ID | ord-1062eafbd8514691beed719cb2ae853b |
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| 出典メモ | uspto-grants-2016_09 |
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