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

HRID 1392145

반응식

HRID 1392145 반응식
[Li+].CC([N-]C(C)C)C.C([Li])CCC.C(NC(C)C)(C)C.[F:21][C:22]1[CH:27]=[CH:26][C:25]([N:28]2[CH2:33][CH2:32][N:31]([S:34]([CH3:37])(=[O:36])=[O:35])[CH2:30][CH2:29]2)=[CH:24][CH:23]=1.[Cl:38][CH2:39][CH2:40][CH2:41][CH2:42][C:43](Cl)=[O:44]>C1COCC1.CCOC(C)=O>[Cl:38][CH2:39][CH2:40][CH2:41][CH2:42][C:43](=[O:44])[CH2:37][S:34]([N:31]1[CH2:32][CH2:33][N:28]([C:25]2[CH:24]=[CH:23][C:22]([F:21])=[CH:27][CH:26]=2)[CH2:29][CH2:30]1)(=[O:35])=[O:36]

참가 물질

8

반응 조건

온도
-78 °C

실험 절차

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+).

후처리

  1. stirringThe mixture was stirred at −78° C. for 1 h and at room temperature for 18 h
  2. washwashed with sat. NH4Cl and brine
  3. dry with materialdried over MgSO4

출처 및 근거

ORD 기록
ord-80a9d8941d6b4987bc430332e5d8dc54
출처 데이터셋
uspto-grants-2008_03
특허 번호
US07342020B2

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