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Methanol → 2-Amino-5-chloro-3-methoxypyrazine

HRID 1107467
ノート
印刷プレビュー

反応式

HRID 1107467 の反応式
[Na].[NH2:2][C:3]1[C:8](Br)=[N:7][C:6]([Cl:10])=[CH:5][N:4]=1.[OH2:11].[CH3:12]O>>[NH2:2][C:3]1[C:8]([O:11][CH3:12])=[N:7][C:6]([Cl:10])=[CH:5][N:4]=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 4

HCID 887MethanolHCID 962WaterHCID 5360545SodiumHCID 104886093-Bromo-5-chloropyrazin-2-amine

生成物 1

HCID 107970362-Amino-5-chloro-3-methoxypyrazine

実験手順

Sodium (2.82 g) was dissolved in dry methanol (50 ml) under argon and 2-amino-3-bromo-5-chloropyrazine (1.68 g) was added in small portions with stirring. The stirred solution was heated at reflux under an atmosphere of argon for 4 hours. The solution was allowed to cool to ambient temperature and water (10 ml) was added. Volatile material was removed by evaporation and water (10 ml) was added to the residue. The mixture was extracted with dichloromethane (3×50 ml) and the combined extracts were dried (MgSO4) and evaporated to give 2-amino-5-chloro-3-methoxypyrazine (1.28 g), m.p. 102-103° C.; 1H NMR (d6 -DMSO): 3.90 (s, 3H), 7.53 (s, 1H); mass spectrum (+ve CI): 160 (M+H)+.

後処理

  1. temperatureThe stirred solution was heated
  2. temperatureat reflux under an atmosphere of argon for 4 hours
  3. customVolatile material was removed by evaporation and water (10 ml)
  4. additionwas added to the residue
  5. extractionThe mixture was extracted with dichloromethane (3×50 ml)
  6. dry with materialthe combined extracts were dried (MgSO4)
  7. customevaporated

出典と根拠

ORDレコード
ord-08e1b076b4574af89cff437f058b09bf
出典データセット
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06060475

反応ノート

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