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HRID 1392145作成日:2026年10月27日

Diisopropylamine → 1-(6-Chloro-2-hexanone-1-sulfonyl)-4-(4-fluorophenyl)piperazine

https://huagongshe.com/reaction/1392145

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylamineHCID 7912—
反応物5-Chlorovaleryl chlorideHCID 74089—
反応物1-(4-Fluorophenyl)-4-(methylsulfonyl)piperazineHCID 669039—
反応物Lithium diisopropylamideHCID 2724682—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物1-(6-Chloro-2-hexanone-1-sulfonyl)-4-(4-fluorophenyl)piperazineHCID 2271972160%

反応条件

温度-78 °C

反応手順

To a solution of LDA (51 mmol, prepared by slow addition of n-butyl lithium (20.4 ml, 2.5M in hexane, 51 mmol) to a solution of diisopropylamine (5.16 g, 51 mmol) in THF (30 ml) at −78° C.) at −78° C. was added a solution of 1-(4-fluorophenyl)-4-(methanesulfonyl)-piperazine (6 g, 23.2 mmol) in THF (150 ml). The mixture was stirred for 1 h at −78° C. A solution of 5-chlorovaleryl chloride (4 g, 25.8 mmol) in THF (20 ml) was added dropwise. The mixture was stirred at −78° C. for 1 h and at room temperature for 18 h. The solution was diluted with EtOAc and washed with sat. NH4Cl and brine and dried over MgSO4. Chromatography of the residue on silica gel (eluant:EtOAc—CH2Cl2—petroleum ether (15:35:50)) afforded 1-(6-chloro-2-hexanone-1-sulfonyl)-4-(4-fluorophenyl)piperazine (5.22 g, 60%) as white crystals: MS (ESI): 399 (MNa+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07342020B2
出典データセットuspto-grants-2008_03
ORD IDord-80a9d8941d6b4987bc430332e5d8dc54
出典メモuspto-grants-2008_03