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2,5-Dibromopyridine → 1-(5-Bromopyridin-2-yl)-4-isopropylpiperazine

HRID 1726873
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인쇄 미리보기

반응식

HRID 1726873 반응식
Br[C:2]1[CH:7]=[CH:6][C:5]([Br:8])=[CH:4][N:3]=1.[CH:9]([N:12]1[CH2:17][CH2:16][NH:15][CH2:14][CH2:13]1)([CH3:11])[CH3:10].C1CCN2C(=NCCC2)CC1>O>[Br:8][C:5]1[CH:6]=[CH:7][C:2]([N:15]2[CH2:16][CH2:17][N:12]([CH:9]([CH3:11])[CH3:10])[CH2:13][CH2:14]2)=[N:3][CH:4]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 693532,5-DibromopyridineHCID 780131-IsopropylpiperazineHCID 811841,8-Diazabicyclo(5.4.0)undec-7-ene

생성물 1

HCID 199958461-(5-Bromopyridin-2-yl)-4-isopropylpiperazine

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
100 °C

실험 절차

A solution containing 12.1 g of 2,5-dibromopyridine (51.1 mmol), 8.8 ml of 1-isopropylpiperazine (61.5 mmol) and 9.2 ml of DBU (61.5 mmol) is stirred overnight at 100° C. The reaction mixture is returned to ambient temperature and the solution is diluted with water and extracted with ethyl acetate. The organic phases are collected, washed with brine, dried (MgSO4) and evaporated under reduced pressure. The residue is chromatographed on an SiO2 column, eluting with a mixture of CH2Cl2/MeOH 98/2 and then 96/4, to yield the title product.

후처리

  1. customis returned to ambient temperature
  2. extractionextracted with ethyl acetate
  3. customThe organic phases are collected
  4. washwashed with brine
  5. dry with materialdried (MgSO4)
  6. customevaporated under reduced pressure
  7. customThe residue is chromatographed on an SiO2 column
  8. washeluting with a mixture of CH2Cl2/MeOH 98/2

출처 및 근거

ORD 기록
ord-e240ed1691f74b2eb57b46dcd73a987c
출처 데이터셋
uspto-grants-2009_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07494995B2

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