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HRID 7653作成日:2026年10月24日

1-Phenethylamine, (-)- → 6-dimethylamino-2-(4-fluorophenyl)-3-[2-(1-(S)-phenylethylamino)-pyrimidin-4yl]-6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-1-one

https://huagongshe.com/ja/reaction/7653

反応式

関与物質

役割名称HCID仕込み量
反応物1-Phenethylamine, (-)-HCID 75818—
反応物6-dimethylamino-2-(4-fluorophenyl)-3-(2-methanesulfonyl-pyrimidin-4-yl)-6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-1-oneHCID 21992208—
溶媒TolueneHCID 1140—
生成物6-dimethylamino-2-(4-fluorophenyl)-3-[2-(1-(S)-phenylethylamino)-pyrimidin-4yl]-6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-1-oneHCID 12133108—

反応条件

温度140 °C

反応手順

A solution of the crude 6-dimethylamino-2-(4-fluorophenyl)-3-(2-methanesulfonyl-pyrimidin-4-yl)-6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-1-one, 25, prepared as described herein above (4.2 g, 10 mmol) and (S)-(−)-α-methyl-benzyl amine (45.2 mL, 351 mmol) are dissolved in toluene (100 mL). The resulting mixture is heated to 140° C. for 12 hours, cooled to room temperature and the solvent removed in vacuo. The resulting residue is purified over silica (1:1 EtOAc/hexanes) to afford the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087615B2
出典データセットuspto-grants-2006_08
ORD IDord-d25374737a9e4104a2fb69a179eedfcd
出典メモuspto-grants-2006_08