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Triethylamine → 3,5-Bis-trimethylsilanylethynyl-pyrazin-2-ylamine

HRID 547467
ノート
印刷プレビュー

反応式

HRID 547467 の反応式
[CH3:1][Si:2]([C:5]#[CH:6])([CH3:4])[CH3:3].NC1C(Br)=[N:12][CH:11]=[C:10](Br)[N:9]=1.[CH2:16]([N:18](CC)CC)[CH3:17]>O1CCCC1.C(OCC)(=O)C.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[Cu]I>[CH3:1][Si:2]([CH3:4])([CH3:3])[C:5]1[C:6]([NH:18][C:16]#[CH:17])=[N:12][CH:11]=[C:10]([Si:2]([CH3:4])([CH3:3])[CH3:1])[N:9]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 3

HCID 8471TriethylamineHCID 66111Trimethylsilylacetylene2 回HCID 510516652-Amino-3,6-dibromopyrazine

生成物 1

HCID 866336003,5-Bis-trimethylsilanylethynyl-pyrazin-2-ylamine収率 82.7%

試薬・触媒・溶媒 4

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)触媒2 回
HCID 178418476
HCID 178418476、化合物
触媒
2 回
HCID 8028Tetrahydrofuran溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

Trimethylsilylacetylene (11.1 mL, 80 mmol) was added to a solution of 2-amino-3,6-dibromopyrazine (5.06 g, 20 mmol), Pd(PPh3)2Cl2 (0.140 g, 0.20 mmol), triethylamine (11.4 mL, 80 mmol) and copper(I) iodide (0.114 g, 0.60 mmol) in 50 mL of tetrahydrofuran at 0-5° C. The reaction mixture was allowed to warm to RT and stirred for 64 h. Additional trimethylsilylacetylene (5.6 mL, 40 mmol), Pd(PPh3)2Cl2 (0.140 g, 0.20 mmol) and copper(I) iodide (0.114 g, 0.60 mmol) were added, and the mixture was stirred at 50° C. for 22 h then allowed to cool to RT. The mixture was diluted with 200 mL of ethyl acetate and 200 mL of hexanes, then sequentially washed with three 200 mL portions of water and 200 mL of a sat. aq. NaHCO3 solution, dried over MgSO4, filtered and concentrated to a residue. Silica gel chromatography (0->25% EtOAc/hexanes) afforded 4.36 g (76%) of 3,5-bis-trimethylsilanylethynyl-pyrazin-2-ylamine as a brown oil.

後処理

  1. stirringthe mixture was stirred at 50° C. for 22 h
  2. temperatureto cool to RT
  3. washsequentially washed with three 200 mL portions of water and 200 mL of a sat. aq. NaHCO3 solution
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated to a residue

出典と根拠

ORDレコード
ord-0a4e2282fefb46cba0c97779cead2bd4
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07939531B2

反応ノート

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