Water → 3-Methyl-4-(piperazin-1-yl)benzonitrile

HRID 716332노트

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HRID 716332 반응식
F[C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][C:3]=1[CH3:10].[NH:11]1[CH2:16][CH2:15][NH:14][CH2:13][CH2:12]1.O>CS(C)=O>[CH3:10][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:2]=1[N:11]1[CH2:16][CH2:15][NH:14][CH2:13][CH2:12]1)[C:6]#[N:7]

참가 물질

5

반응물 3

HCID 962WaterHCID 4837PiperazineHCID 27791804-Fluoro-3-methylbenzonitrile

생성물 1

HCID 600511423-Methyl-4-(piperazin-1-yl)benzonitrile수율 69.6%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

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온도
140 °C

실험 절차

To a solution of 4-fluoro-3-methylbenzonitrile (2.5 g, 18.50 mmol) in DMSO (Volume: 10.0 mL) was added piperazine (7.97 g, 92 mmol) at 23° C. The reaction was stirred at 140° C. for 16 hr. The reaction mixture was poured into H2O (100 mL) and the reaction vessel was rinsed with H2O (˜50 mL). The resulting suspension was filtered, rinsed with H2O (3×10 mL) and the resulting solid was dried in vacuo to provide 3-methyl-4-(piperazin-1-yl)benzonitrile (2.593 g, 12.88 mmol, 69.6% yield) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 2.21-2.30 (m, 3H) 2.57-2.70 (m, 1H) 2.83 (s, 8H) 7.03-7.09 (m, 1H) 7.55-7.62 (m, 2H). ESI-MS: m/z 202.1 (M+H)+.

후처리

  1. washthe reaction vessel was rinsed with H2O (˜50 mL)
  2. filtrationThe resulting suspension was filtered
  3. washrinsed with H2O (3×10 mL)
  4. customthe resulting solid was dried in vacuo

출처 및 근거

ORD 기록
ord-0250d665b1e64625b2375da3c10e83c3
출처 데이터셋
uspto-grants-2015_11
특허 번호
US09187497B2

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