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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1582058생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1582058

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물5-Chlorovaleryl chlorideHCID 74089—
반응물1-(4-Fluorophenyl)-4-(methylsulfonyl)piperazineHCID 669039—
반응물Lithium diisopropylamideHCID 2724682—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물1-(6-Chloro-2-hexanone-1-sulfonyl)-4-(4-fluorophenyl)piperazineHCID 2271972160%

반응 조건

온도-78 °C

반응 단계

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+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06734184B1
출처 데이터셋uspto-grants-2004_05
ORD IDord-09a5bc7c7a6b48a7be2af349fbdf7e13
출처 메모uspto-grants-2004_05