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1-Butyne, 3-chloro-3-methyl- → 1-[1,1-Dimethylethoxycarbonyl]-4-[3-(1,1-dimethylprop-2-ynylamino)-2-pyridinyl]piperazine

HRID 2293765
ノート
印刷プレビュー

反応式

HRID 2293765 の反応式
[CH3:1][C:2]([CH3:20])([O:4][C:5]([N:7]1[CH2:12][CH2:11][N:10]([C:13]2[C:18]([NH2:19])=[CH:17][CH:16]=[CH:15][N:14]=2)[CH2:9][CH2:8]1)=[O:6])[CH3:3].Cl[C:22]([CH3:26])([CH3:25])[C:23]#[CH:24]>CN(C)C=O.[Cu]>[CH3:3][C:2]([CH3:20])([O:4][C:5]([N:7]1[CH2:8][CH2:9][N:10]([C:13]2[C:18]([NH:19][C:22]([CH3:26])([CH3:25])[C:23]#[CH:24])=[CH:17][CH:16]=[CH:15][N:14]=2)[CH2:11][CH2:12]1)=[O:6])[CH3:1]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 706791-Butyne, 3-chloro-3-methyl-HCID 2756375tert-Butyl 4-(3-aminopyridin-2-yl)piperazine-1-carboxylate

生成物 1

HCID 214776701-[1,1-Dimethylethoxycarbonyl]-4-[3-(1,1-dimethylprop-2-ynylamino)-2-pyridinyl]piperazine

試薬・触媒・溶媒 2

HCID 23978Copper触媒HCID 6228Dimethylformamide溶媒2 回

実験手順

To a mixture of 1-[1,1-dimethylethoxycarbonyl]-4-[3-amino-2-pyridinyl]piperazine (International Publication No. WO 88/08424, 5.40 g), cuprous chloride (1.00 g), copper powder (1.00 g), and dry dimethylformamide (25 ml) under nitrogen at 0° is added a solution of 3-chloro-3-methyl-1-butyne (2.00 g) in dry dimethylformamide (5 ml) in 4 portions over 15 min. The resulting mixture is then stirred at 20°-25° for 16 hrs, concentrated, and diluted with methylene chloride (75 ml) and water (20 ml). The layers are separated and the aqueous phase is extracted with methylene chloride (25 ml). The combined organic phase is washed with saline (20 ml), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give a residue which is chromatographed on silica gel (70-230 mesh, 500 g), eluting with a gradient of ethyl acetate/hexane (10/90-20/80). Pooling of fractions giving an Rf =0.31 (ethyl acetate/hexane, 25/75) and removal of solvent under reduced pressure gives the title compound, NMR (CDCl3) 7.75, 7.47, 6.94, 4.61, 3.56, 3.00, 2.39, 1.64 and 1.48 δ.

後処理

  1. concentrationconcentrated
  2. additiondiluted with methylene chloride (75 ml) and water (20 ml)
  3. customThe layers are separated
  4. extractionthe aqueous phase is extracted with methylene chloride (25 ml)
  5. washThe combined organic phase is washed with saline (20 ml)
  6. dry with materialdried over anhydrous magnesium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customto give a residue which
  9. customis chromatographed on silica gel (70-230 mesh, 500 g)
  10. washeluting with a gradient of ethyl acetate/hexane (10/90-20/80)
  11. customPooling of fractions giving
  12. customan Rf =0.31 (ethyl acetate/hexane, 25/75) and removal of solvent under reduced pressure

出典と根拠

ORDレコード
ord-c1f035efdef44dbb897c17d3c0195a10
出典データセット
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05686610

反応ノート

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