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HRID 2125作成日:2026年10月23日

Hexane → 5-(4-Chlorophenyl)-1-(2-pentyn-1-yl)-2-pyrimidinone

https://huagongshe.com/ja/reaction/2125

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物2-PyridoneHCID 8871—
反応物Sodium hydrideHCID 24758—
反応物Ammonium ChlorideHCID 25517—
反応物1-Bromopent-2-yneHCID 85399—
溶媒DimethylformamideHCID 6228—
生成物5-(4-Chlorophenyl)-1-(2-pentyn-1-yl)-2-pyrimidinoneHCID 18917051—

反応条件

温度0 °C

反応手順

To a suspension of NaH (60% in mineral oil, 340 mg) in dry DMF (75 ml) at 0° C. was added the preceding pyridinone (1.0 g) and the mixture was stirred at 0° C. for one half hour. To the resulting suspension was added 1-bromo-2-pentyne (750 mg) dropwise. The resulting mixture was kept at 0° C. for one half hour and poured into saturated aqueous ammonium chloride (200 ml). The aqueous suspension was extracted with ether (3×100 ml), the combined ether layers washed with brine and dried, yielding the crude product. Trituration with hexane yielded the product as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728698
出典データセットuspto-grants-1998_03
ORD IDord-b6e9c38f760d411e813e29218db44408
出典メモuspto-grants-1998_03