2-Aminopyridine → HCID 178515422、化合物

HRID 1112522ノート

反応式

HRID 1112522 の反応式
[Cl-].[Al+3].[Cl-].[Cl-].[N-:5]=[N+:6]=[N-:7].[Na+].[NH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][N:11]=1.C([O:18][CH:19]=[C:20]([C:26]#[N:27])[C:21](OCC)=O)C>O1CCCC1>[NH:5]1[C:26]([C:20]2[C:19](=[O:18])[N:11]3[CH:12]=[CH:13][CH:14]=[CH:15][C:10]3=[N:9][CH:21]=2)=[N:27][N:7]=[N:6]1

参加物

6

実験手順

Aluminum chloride (1.73 g., 12.96 mmoles) was added to tetrahydrofuran (45 ml.) at -20°. Sodium azide (2.52 g., 38.71 mmoles) was then added and the mixture heated under reflux for 40 minutes. To this mixture was added 2-aminopyridine (1.0 g., 10.62 mmoles) and ethyl ethoxymethylenecyanoacetate (1.8 g., 10.62 mmoles). The mixture was heated under reflux for 18 hours. The mixture was concentrated and the residue treated with water (50 ml.). The mixture was acidified to pH 3 with 6N hydrochloric acid. The solid material was collected and suspended in 3% aqueous sodium bicarbonate. The mixture was heated under reflux for 5 minutes, filtered, and the filtrate acidified to pH 4 with 6N hydrochloric acid. The precipitate was recrystallized from N,N-dimethylformamide to give the title compound (0.35 g., 15.4%), m.p. 312°-313° (decomp).

後処理

  1. temperaturethe mixture heated
  2. temperatureunder reflux for 40 minutes
  3. temperatureThe mixture was heated
  4. temperatureunder reflux for 18 hours
  5. concentrationThe mixture was concentrated
  6. additionthe residue treated with water (50 ml.)
  7. customThe solid material was collected
  8. temperatureThe mixture was heated
  9. temperatureunder reflux for 5 minutes
  10. filtrationfiltered
  11. customThe precipitate was recrystallized from N,N-dimethylformamide

出典と根拠

ORDレコード
ord-6cfd725b15ab41829db020e49e195d80
出典データセット
uspto-grants-1978_10
特許番号
US04122274

反応ノート

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