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Triethylamine → Tert-butyl 4-{5-[(trimethylsilyl)ethynyl]pyridin-2-yl}piperazine-1-carboxylate

HRID 859917
ノート
印刷プレビュー

反応式

HRID 859917 の反応式
I[C:2]1[CH:3]=[CH:4][C:5]([N:8]2[CH2:13][CH2:12][N:11]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH2:10][CH2:9]2)=[N:6][CH:7]=1.[CH3:21][Si:22]([C:25]#[CH:26])([CH3:24])[CH3:23].C(N(CC)CC)C>CC(N(C)C)=O>[CH3:21][Si:22]([C:25]#[C:26][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[CH2:13][CH2:12][N:11]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH2:10][CH2:9]2)=[N:6][CH:7]=1)([CH3:24])[CH3:23]
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 3

HCID 8471TriethylamineHCID 66111TrimethylsilylacetyleneHCID 7164639tert-Butyl 4-(5-iodopyridin-2-yl)piperazine-1-carboxylate

生成物 1

HCID 69606761Tert-butyl 4-{5-[(trimethylsilyl)ethynyl]pyridin-2-yl}piperazine-1-carboxylate収率 70.4%

試薬・触媒・溶媒 1

HCID 31374Dimethylacetamide溶媒

実験手順

To a stirred solution of tert-butyl 4-(5-iodopyridin-2-yl)piperazine-1-carboxylate (1.0 g, 2.57 mmol, prepared as in Example 1), trimethylsilyl acetylene (0.73 mL, 5.14 mmol), triethylamine (1.11 mL, 7.71 mmol), and cuprous iodide (196 mg, 1.03 mmol) in DMA (20 mL) at 25° C. was added tetrakistriphenylphosphine palladium (0) (149 mg, 5 mol %). The reaction was stirred for 10 minutes. Volatiles were removed in vacuo. The residue was then dissolved in ethyl acetate (250 mL) and washed with water (100 mL). The layers were then separated and the aqueous phase extracted with ethyl acetate (250 mL). The combined organic extracts were then dried, (MgSO4), filtered and concentrated in vacuo. The residue was then purified by flash chromatography (silica gel, 10% EtOAc in hexanes) to give tert-butyl 4-{5-[(trimethylsilyl)ethynyl]pyridin-2-yl}piperazine-1-carboxylate as a pale brown solid (652 mg, 1.81 mmol, 70%).

後処理

  1. customVolatiles were removed in vacuo
  2. dissolutionThe residue was then dissolved in ethyl acetate (250 mL)
  3. washwashed with water (100 mL)
  4. customThe layers were then separated
  5. extractionthe aqueous phase extracted with ethyl acetate (250 mL)
  6. dry with materialThe combined organic extracts were then dried, (MgSO4),
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customThe residue was then purified by flash chromatography (silica gel, 10% EtOAc in hexanes)

出典と根拠

ORDレコード
ord-088d98d42a744e67a75c49cdac7dabc7
出典データセット
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07153857B2

反応ノート

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