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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

反応式

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}acetamideHCID 11183866—
反応物HCID 178509389HCID 178509389—
溶媒Acetic AcidHCID 176—
生成物N-(3-(3-cyano-2-(4-phenoxyphenyl)pyrazolo[1,5-a]pyrimidin-7-yl)phenyl)acetamideHCID 11766810490%

反応条件

温度118 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447106B2
出典データセットuspto-grants-2016_09
ORD IDord-1062eafbd8514691beed719cb2ae853b
出典メモuspto-grants-2016_09