Acetic Acid → 1-Benzyl-4-[3-(1-cyano-1-methylethylamino)pyridyl]-piperazine

HRID 1449743ノート

反応式

HRID 1449743 の反応式
N[C:2]1C=[C:4]2[C:8](=[CH:9][CH:10]=1)N[C:6]([N:11]1[CH2:16][CH2:15][N:14]([C:17]3[C:22]([NH:23]C(C)C)=[CH:21][CH:20]=[CH:19][N:18]=3)[CH2:13][C:12]1=C=O)=[CH:5]2.[CH3:29]C(C)=O.C[Si]([C:37]#[N:38])(C)C.[OH-].[Na+].[C:41](O)(=O)[CH3:42]>CO.C(OCC)(=O)C.CCCCCC>[CH2:6]([N:11]1[CH2:12][CH2:13][N:14]([C:17]2[C:22]([NH:23][C:41]([C:37]#[N:38])([CH3:42])[CH3:29])=[CH:21][CH:20]=[CH:19][N:18]=2)[CH2:15][CH2:16]1)[C:5]1[CH:2]=[CH:10][CH:9]=[CH:8][CH:4]=1

参加物

8

実験手順

The 1-[5-Aminoindolyl -2-carbonyl -4-[3-(1-methylethyl amino)-2-pyridinyl]piperazine (EXAMPLE 7, 11.68 g, 43.51 mmol) is dissolved in 130 ml methanol and 130 ml acetic acid. Acetone (25.6 ml, 348.1 mmol) and trimethylsilylcyanide (46.4 ml, 348.1 mmol) are added and the mixture is stirred twenty hours. The solution is poured into cold aqueous sodium hydroxide solution, stirring vigorously, to give a basic solution. The aqueous solution is then extracted with ethyl acetate, the organic extract is washed with saline, dried over sodium sulfate and evaporated to dryness to give an oily residue of 12.6 g. Chromatography on a 400 g silica gel column with a step gradient of ethyl acetate/hexane (2/3 to 3/2, v/v), pooling and concentrating the appropriate fractions gives the title compound, NMR (300 MHz, CD3OD) 7.65, 7.29-7.17, 6.96-6.92, 3.51, 2.98, 2.55, 1.14 δ.

後処理

  1. stirringstirring vigorously
  2. customto give a basic solution
  3. extractionThe aqueous solution is then extracted with ethyl acetate
  4. extractionthe organic extract
  5. washis washed with saline
  6. dry with materialdried over sodium sulfate
  7. customevaporated to dryness
  8. customto give an oily residue of 12.6 g
  9. concentrationconcentrating the appropriate fractions

出典と根拠

ORDレコード
ord-a69ed5980bcc44098a9634312844006e
出典データセット
uspto-grants-1997_02
特許番号
US05599930

反応ノート

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