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Piperazine → 2-(6-Piperazin-1-YL-pyridin-3-YL)-1H-benzoimidazole

HRID 499156
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HRID 499156 반응식
Cl[C:2]1[N:7]=[CH:6][C:5]([C:8]2[NH:12][C:11]3[CH:13]=[CH:14][CH:15]=[CH:16][C:10]=3[N:9]=2)=[CH:4][CH:3]=1.[NH:17]1[CH2:22][CH2:21][NH:20][CH2:19][CH2:18]1>CN1CCCC1=O>[N:17]1([C:2]2[N:7]=[CH:6][C:5]([C:8]3[NH:12][C:11]4[CH:13]=[CH:14][CH:15]=[CH:16][C:10]=4[N:9]=3)=[CH:4][CH:3]=2)[CH2:22][CH2:21][NH:20][CH2:19][CH2:18]1
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참가 물질

4

반응물 2

HCID 4837PiperazineHCID 14883902-(6-chloropyridin-3-yl)-1H-1,3-benzodiazole

생성물 1

HCID 675232322-(6-Piperazin-1-YL-pyridin-3-YL)-1H-benzoimidazole수율 93%

시약·촉매·용매 1

HCID 13387N-methyl-2-pyrrolidone용매

반응 조건

온도
140 °C

실험 절차

A mixture of 2-(6-chloropyridin-3-yl)-1H-benzoimidazole (0.468 g, 2.040 mmol) and piperazine (0.516 g, 6.000 mmol) in 1-methyl-2-pyrrolidone was heated to 140° C. with stirring for 2 hours. The solvent was removed in vacuo. The residue was diluted with water (100 mL) and stirred for 15 minutes. A white precipitate was formed which was collected by filtration and dried to afford the title compound in 93% yield (0.529 g, 1.900 mmol).

후처리

  1. customThe solvent was removed in vacuo
  2. additionThe residue was diluted with water (100 mL)
  3. stirringstirred for 15 minutes
  4. customA white precipitate was formed which
  5. filtrationwas collected by filtration
  6. customdried

출처 및 근거

ORD 기록
ord-dc0cb6459b17461a832638e28ded9bcc
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07767677B2

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