Hydrochloric Acid → Dapivirine

HRID 2305421ノート

反応式

HRID 2305421 の反応式
Cl[C:2]1[N:7]=[C:6]([NH:8][C:9]2[C:14]([CH3:15])=[CH:13][C:12]([CH3:16])=[CH:11][C:10]=2[CH3:17])[CH:5]=[CH:4][N:3]=1.Cl.CC(O)C.[NH2:23][C:24]1[CH:31]=[CH:30][C:27]([C:28]#[N:29])=[CH:26][CH:25]=1.C([O-])(O)=O.[Na+]>O>[CH3:17][C:10]1[CH:11]=[C:12]([CH3:16])[CH:13]=[C:14]([CH3:15])[C:9]=1[NH:8][C:6]1[CH:5]=[CH:4][N:3]=[C:2]([NH:23][C:24]2[CH:31]=[CH:30][C:27]([C:28]#[N:29])=[CH:26][CH:25]=2)[N:7]=1

参加物

7

反応条件

温度
42.5 °C

実験手順

A mixture of intermediate 49 (0.082 mol) and 5.4 N HCl in 2-propanol (0.086 mol) in water (300 ml) was stirred and warmed to 40-45° C. over 30 minutes. 4-Amino-benzonitrile (0.242 mol) was added at 40-45° C. The reaction mixture was stirred and refluxed for 4.5 hours, then cooled to room temperature. The mixture was alkalized by portionwise addition of NaHCO3. This mixture was extracted with ethylacetate. The organic layer was separated, washed with brine, dried, filtered, and the solvent was evaporated. This fraction was stirred in ethanol p.a. (100 ml), filtered off, washed with ethanol (50 ml), then dried, yielding 23.1 g (86%) 4-[[4-[(2,4,6-trimethylphenyl)amino]-2-pyrimidinyl]amino]benzonitrile (compound 52).

後処理

  1. stirringThe reaction mixture was stirred
  2. temperaturerefluxed for 4.5 hours
  3. temperaturecooled to room temperature
  4. extractionThis mixture was extracted with ethylacetate
  5. customThe organic layer was separated
  6. washwashed with brine
  7. customdried
  8. filtrationfiltered
  9. customthe solvent was evaporated
  10. stirringThis fraction was stirred in ethanol p.a
  11. filtration(100 ml), filtered off
  12. washwashed with ethanol (50 ml)
  13. customdried

出典と根拠

ORDレコード
ord-c07c41ce77d9461e843893d6efe37bb3
出典データセット
uspto-grants-2002_08
特許番号
US06440986B2

反応ノート

読み込み中…