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2,5-Hexanedione → 1-[3-Bromo-5-(2,5-dimethylpyrrol-1-yl)-4-pyridyl]-4-methyl-piperazine

HRID 524897
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HRID 524897 반응식
[Br:1][C:2]1[C:3]([N:9]2[CH2:14][CH2:13][N:12]([CH3:15])[CH2:11][CH2:10]2)=[C:4]([NH2:8])[CH:5]=[N:6][CH:7]=1.[CH3:16][C:17](=O)[CH2:18][CH2:19][C:20](=O)[CH3:21]>C(O)(=O)C>[Br:1][C:2]1[CH:7]=[N:6][CH:5]=[C:4]([N:8]2[C:20]([CH3:21])=[CH:19][CH:18]=[C:17]2[CH3:16])[C:3]=1[N:9]1[CH2:14][CH2:13][N:12]([CH3:15])[CH2:11][CH2:10]1
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참가 물질

4

반응물 2

HCID 80352,5-HexanedioneHCID 867209525-Bromo-4-(4-methylpiperazin-1-yl)pyridin-3-amine

생성물 1

HCID 867209531-[3-Bromo-5-(2,5-dimethylpyrrol-1-yl)-4-pyridyl]-4-methyl-piperazine

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

5-bromo-4-(4-methylpiperazin-1-yl)pyridin-3-amine (3000 mg, 11.06 mmol), hexane-2,5-dione (6.312 g, 6.487 mL, 55.30 mmol) in acetic acid (20 mL) was heated at 70° C. overnight. The reaction mixture was concentrated in vacuo and the residue was partitioned between EtOAc and an aqueous saturated solution of NaHCO3. Combined organic extract was washed with brine, dried (MgSO4) and concentrated in vacuo yielding an oil that was purified by filtration on silica to yield 1-(3-bromo-5-(2,5-dimethyl-1H-pyrrol-1-yl)pyridin-4-yl)-4-methylpiperazine as an off-white solid. MS (ES+) 351.1.

후처리

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. customthe residue was partitioned between EtOAc
  3. extractionCombined organic extract
  4. washwas washed with brine
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated in vacuo
  7. customyielding an oil that
  8. filtrationwas purified by filtration on silica

출처 및 근거

ORD 기록
ord-6ca67994b9844a248a37566184c34a58
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09340546B2

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