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Hydrochloric Acid → 2-Bromo-5-methoxypyrazine

HRID 1587671
ノート
印刷プレビュー

反応式

HRID 1587671 の反応式
Cl.N[C:3]1[CH:8]=[N:7][C:6]([Br:9])=[CH:5][N:4]=1.N([O:12][CH2:13]CC(C)C)=O>CO>[Br:9][C:6]1[CH:5]=[N:4][C:3]([O:12][CH3:13])=[CH:8][N:7]=1
参加物反応条件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 313Hydrochloric AcidHCID 8053Isoamyl NitriteHCID 5995392-Amino-5-bromopyrazine

生成物 1

HCID 197561722-Bromo-5-methoxypyrazine収率 85.3%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
-10 °C

実験手順

Methanolic hydrogen chloride (0.8 mL of a 10M methanolic solution) was added to a stirred solution of 2-amino-5-bromopyrazine (6.96 g, 0.04 mol) in anhydrous methanol (125 mL). To this cooled (-10° C.) solution was added isoamyl nitrite (16.1 mL, 0.12 mol) and the reaction mixture was stirred at -10° C. for 1.5 hours then at room temperature for 2 hours. The solvent was evaporated and the residue partitioned between aqueous saturated sodium carbonate (50 mL) and dichloromethane (4×50 mL). The combined organics were dried (sodium carbonate) and evaporated to give a brown oil which was purified by column chromatography on silica using 5% ethyl acetate in petroleum ether (60-80) to afford 2-bromo-5-methoxypyrazine as a pale yellow solid (6.45 g, 85%).

後処理

  1. waitat room temperature for 2 hours
  2. customThe solvent was evaporated
  3. customthe residue partitioned between aqueous saturated sodium carbonate (50 mL) and dichloromethane (4×50 mL)
  4. dry with materialThe combined organics were dried (sodium carbonate)
  5. customevaporated
  6. customto give a brown oil which
  7. customwas purified by column chromatography on silica using 5% ethyl acetate in petroleum ether (60-80)

出典と根拠

ORDレコード
ord-a69ea8dd4b9e40b38f55e49247087c95
出典データセット
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05219849

反応ノート

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