Sodium Chloride → 6-Amino-2-pyridinemethanol

HRID 34785

反応式

HRID 34785 の反応式
[NH2:1][C:2]1[N:7]=[C:6]([C:8](O)=[O:9])[CH:5]=[CH:4][CH:3]=1.B.[OH-].[Na+].[Cl-].[Na+]>O1CCCC1>[NH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]([CH2:8][OH:9])[N:7]=1

参加物

6

実験手順

A mixture of 6-aminopyridine-2-carboxylic acid (5.0 g.) and a 1.35M solution of borane in tetrahydrofuran (100 ml.) was stirred under argon at reflux for 48 hours. The mixture was cooled and treated with 2N NaOH (50 ml.) and the mixture stirred at room temperature for 18 hours. The aqueous phase was saturated with sodium chloride and the organic phase separated. The aqueous phase was extracted twice with ethyl acetate and the ethyl acetate extracts combined with the tetrahydrofuran solution and the whole evaporated to dryness. The residue was dissolved in ethyl acetate (100 ml.) and the solution washed with saturated aqueous sodium chloride solution (5 ml.) and then dried and evaporated to dryness to give crude 2-amino-6-hydroxymethylpyridine (2.3 g.) which was used without further purification.

後処理

  1. temperatureat reflux for 48 hours
  2. temperatureThe mixture was cooled
  3. customthe organic phase separated
  4. extractionThe aqueous phase was extracted twice with ethyl acetate
  5. customthe whole evaporated to dryness
  6. dissolutionThe residue was dissolved in ethyl acetate (100 ml.)
  7. washthe solution washed with saturated aqueous sodium chloride solution (5 ml.)
  8. customdried
  9. customevaporated to dryness

出典と根拠

ORDレコード
ord-9bb7bd1776e046e88e983a31e7d7df70
出典データセット
uspto-grants-1988_08
特許番号
US04762932

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