Iodobenzene → N2-methyl-N3-phenylpyridine-2,3-diamine

HRID 333562ノート

反応式

HRID 333562 の反応式
[CH3:1][NH:2][C:3]1[C:8]([NH2:9])=[CH:7][CH:6]=[CH:5][N:4]=1.I[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.CC([O-])(C)C.[Na+].C1(P(C2C=CC=CC=2)C2C=CC=C3C=2C(C2C4C(=CC=CC=4P(C4C=CC=CC=4)C4C=CC=CC=4)C=CC=2)=CC=C3)C=CC=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.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd].C1(C)C=CC=CC=1>[CH3:1][NH:2][C:3]1[C:8]([NH:9][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:7][CH:6]=[CH:5][N:4]=1

参加物

7

実験手順

N2-methylpyridine-2,3-diamine (11.95 g, 97 mmol), iodobenzene (16.22 ml, 146 mmol), sodium 2-methylpropan-2-olate (13.99 g, 146 mmol), 8,8′-bis(diphenylphosphino)-1,1′-binaphthalene (BINAP) (60.4 g, 97 mmol) with toluene (400 mL) were added to a three necked 1 L round bottom flask. The reaction was degassed with N2 for 20 minutes. Pd2(dba)3 (1.777 g, 1.941 mmol) was added and the reaction mixture was refluxed for 20 h. The reaction mixture was concentrated to dryness. Residue was dissolved in EtOAc. It was not clear solution, but a suspension was obtained and then filtered through a silica gel plug. The desired product was concentrated and recrystallized from DCM/hexanes providing a yield of 6.45 g, 33.3%.

後処理

  1. customThe reaction was degassed with N2 for 20 minutes
  2. temperaturethe reaction mixture was refluxed for 20 h
  3. concentrationThe reaction mixture was concentrated to dryness
  4. dissolutionResidue was dissolved in EtOAc
  5. customa suspension was obtained
  6. filtrationfiltered through a silica gel plug
  7. concentrationThe desired product was concentrated
  8. customrecrystallized from DCM/hexanes providing a yield of 6.45 g, 33.3%

出典と根拠

ORDレコード
ord-ece73c7210ac4131bad4f9c6528c419a
出典データセット
uspto-grants-2014_11
特許番号
US08883322B2

反応ノート

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