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Acetonitrile → HCID 21298702、化合物

HRID 34818
ノート
印刷プレビュー

反応式

HRID 34818 の反応式
[F:1][C:2]([F:10])([CH:7]([F:9])[F:8])[CH2:3][N:4]=[C:5]=S.C1(=O)[N:15]([CH2:16][CH2:17][CH2:18][S:19][C:20]2[N:25]=[C:24]([NH2:26])[CH:23]=[CH:22][N:21]=2)C(=O)C2=CC=CC=C12.C(#[N:35])C>CN(C)C=O.N>[F:1][C:2]([F:10])([CH:7]([F:9])[F:8])[CH2:3][N:4]=[C:5]([NH2:35])[NH:26][C:24]1[CH:23]=[CH:22][N:21]=[C:20]([S:19][CH2:18][CH2:17][CH2:16][NH2:15])[N:25]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 6342AcetonitrileHCID 212797361,1,2,2-Tetrafluoro-3-isothiocyanatopropaneHCID 21298869HCID 21298869、化合物

生成物 1

HCID 21298702HCID 21298702、化合物

試薬・触媒・溶媒 2

HCID 222Ammonia溶媒HCID 6228Dimethylformamide溶媒

実験手順

2,2,3,3-Tetrafluoropropylisothiocyanate (0.9 g.) and 2-(3-phthalimidopropylthio)-4-aminopyrimidine (0.9 g.) were dissolved in acetonitrile (30 ml.) and heated under reflux for 64 hours. The resulting suspension was cooled, filtered and the collected solid washed with acetonitrile (10 ml.) to give a white solid (0.9 g.). This was dissolved in a mixture of dimethylformamide (10 ml.) and saturated ethanolic ammonia solution (5 ml.) and treated with yellow mercuric oxide (0.8 g.). The mixture was stirred at room temperature for 3 hours. The solvent was evaporated and the black residue was triturated with ethyl acetate and filtered. The solvent was evaporated and the residual gum was dissolved in ethanol (15 ml.) and added to a solution of hydrazine (5 ml.) in ethanol (10 ml.). The mixture was stirred at room temperature for 2 hours then the solvent was evaporated. The residue was triturated with 1N hydrochloric acid, filtered and the filtrate was basified with 10N sodium hydroxide solution. The product was extracted with ethyl acetate, dried (magnesium sulphate) and the solvent was evaporated to give 4-[2-(2,2,3,3-tetrafluoropropyl)guanidino]-2-[3-aminopropylthio]pyrimidine (0.5 g.) which was used without further purification.

後処理

  1. temperatureheated
  2. temperatureunder reflux for 64 hours
  3. temperatureThe resulting suspension was cooled
  4. filtrationfiltered
  5. washthe collected solid washed with acetonitrile (10 ml.)
  6. customto give a white solid (0.9 g.)
  7. customThe solvent was evaporated
  8. customthe black residue was triturated with ethyl acetate
  9. filtrationfiltered
  10. customThe solvent was evaporated
  11. dissolutionthe residual gum was dissolved in ethanol (15 ml.)
  12. additionadded to a solution of hydrazine (5 ml.) in ethanol (10 ml.)
  13. stirringThe mixture was stirred at room temperature for 2 hours
  14. customthe solvent was evaporated
  15. customThe residue was triturated with 1N hydrochloric acid
  16. filtrationfiltered
  17. extractionThe product was extracted with ethyl acetate
  18. dry with materialdried (magnesium sulphate)
  19. customthe solvent was evaporated

出典と根拠

ORDレコード
ord-9f510a33badb4b9bb3f635bdca0641c5
出典データセット
uspto-grants-1988_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04762932

反応ノート

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