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1-Methylpiperazine → 5-(4-Methylpiperazin-1-yl)-2-trifluoromethoxyphenylamine

HRID 1914758
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HRID 1914758 반응식
Br[C:2]1[CH:3]=[CH:4][C:5]([O:9][C:10]([F:13])([F:12])[F:11])=[C:6]([NH2:8])[CH:7]=1.[Li]N([Si](C)(C)C)[Si](C)(C)C.[CH3:24][N:25]1[CH2:30][CH2:29][NH:28][CH2:27][CH2:26]1>C1COCC1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd].C1(P(C2CCCCC2)C2C=CC=CC=2C2C=CC=CC=2N(C)C)CCCCC1>[CH3:24][N:25]1[CH2:30][CH2:29][N:28]([C:2]2[CH:3]=[CH:4][C:5]([O:9][C:10]([F:13])([F:12])[F:11])=[C:6]([NH2:8])[CH:7]=2)[CH2:27][CH2:26]1
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참가 물질

7

반응물 3

HCID 531671-MethylpiperazineHCID 27793675-Bromo-2-(trifluoromethoxy)anilineHCID 178418261HCID 178418261, 화합물

생성물 1

HCID 249941425-(4-Methylpiperazin-1-yl)-2-trifluoromethoxyphenylamine수율 64%

시약·촉매·용매 3

HCID 27342172-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenyl촉매
HCID 9811564
Bis(dibenzylideneacetone)palladium
촉매
HCID 8028Tetrahydrofuran용매

실험 절차

Tris(dibenzilideneacetone)dipalladium, Pd2(dba)3 (1.1 g, 1.2 mmol), 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)-biphenyl (0.94 g, 2.4 mmol), 5-bromo-2-trifluoromethoxy-phenylamine (30.7 g, 120 mmol) in THF (50 mL) were charged in a round-bottom flask flushed with argon. The flask was evacuated and backfilled with argon. LiN(TMS)2 solution (1M in THF, 288 mL) and N-methylpiperazine (26.7 mL, 194 mmol) were added and the reaction refluxed for 1 h. The reaction mixture was then allowed to cool to room temperature and filtered through a pad of celite. The organic phase was concentrated, the residue dissolved in DCM (200 ml) and washed with water (1×100 ml). The organic phases were dried over anhydrous Na2SO4, the solvent evaporated in vacuo and the crude solid was purified by flash chromatography on silica gel (eluant: DCM/EtOH 90/10) to afford 21.1 g of 5-(4-methyl-piperazin-1-yl)-2-trifluoromethoxy-phenylamine (64% yield) as a light brown powder.

후처리

  1. customflushed with argon
  2. customThe flask was evacuated
  3. temperaturethe reaction refluxed for 1 h
  4. filtrationfiltered through a pad of celite
  5. concentrationThe organic phase was concentrated
  6. dissolutionthe residue dissolved in DCM (200 ml)
  7. washwashed with water (1×100 ml)
  8. dry with materialThe organic phases were dried over anhydrous Na2SO4
  9. customthe solvent evaporated in vacuo
  10. customthe crude solid was purified by flash chromatography on silica gel (eluant: DCM/EtOH 90/10)

출처 및 근거

ORD 기록
ord-5c613f3e0c7c44888041ef8056620e2e
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08614220B2

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