Bromine → 2-Bromo-6-methoxypyridin-3-amine

HRID 12307

反応式

HRID 12307 の反応式
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([O:8][CH3:9])=[N:6][CH:7]=1.C([O-])(=O)C.[Na+].[Br:15]Br.S([O-])([O-])(=O)=S.[Na+].[Na+]>C(O)(=O)C>[NH2:1][C:2]1[C:7]([Br:15])=[N:6][C:5]([O:8][CH3:9])=[CH:4][CH:3]=1

参加物

6

反応物 4

HCID 24408BromineHCID 24477Sodium ThiosulfateHCID 811216-Methoxy-3-pyridinylamineHCID 517045Sodium Acetate

生成物 1

HCID 152093242-Bromo-6-methoxypyridin-3-amine

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

A mixture of 1.83 g (14.7 mM) of 5-amino-2-methoxypyridine and 1.21 g (14.7 mM) of sodium acetate in 12 ml of acetic acid is prepared and 0.75 ml (14.7 mM) of bromine is added gently, with stirring and while maintaining at room temperature. The reaction mixture is kept stirring for 30 minutes, at room temperature, and 200 ml of saturated sodium thiosulfate solution are then added. The aqueous phase obtained is extracted twice with ethyl acetate. The combined organic phases are dried over magnesium sulfate and concentrated under reduced pressure. 3 g of the expected compound are obtained in the form of a violet-colored solid (quantitative yield).

後処理

  1. customis prepared
  2. stirringThe reaction mixture is kept stirring for 30 minutes, at room temperature
  3. customThe aqueous phase obtained
  4. extractionis extracted twice with ethyl acetate
  5. dry with materialThe combined organic phases are dried over magnesium sulfate
  6. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-27352282c0af4dfbb16addeee00b36b0
出典データセット
uspto-grants-2010_06
特許番号
US07728002B2

関連ノート

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