Triethylamine → 4-(7-Chloro-1,3-benzodioxol-5-yl)-2-pyrimidin-2-yl-5-(trifluoromethyl)pyrazol-3-amine

HRID 705706

Reaktionsgleichung

Reaktionsgleichung von HRID 705706
Cl[C:2]([C:16]([F:19])([F:18])[F:17])=[C:3]([C:6]1[CH:14]=[C:13]([Cl:15])[C:9]2[O:10][CH2:11][O:12][C:8]=2[CH:7]=1)[C:4]#[N:5].[N:20]1[CH:25]=[CH:24][CH:23]=[N:22][C:21]=1[NH:26][NH2:27].C(N(CC)CC)C>C(O)C>[Cl:15][C:13]1[C:9]2[O:10][CH2:11][O:12][C:8]=2[CH:7]=[C:6]([C:3]2[C:2]([C:16]([F:18])([F:17])[F:19])=[N:27][N:26]([C:21]3[N:22]=[CH:23][CH:24]=[CH:25][N:20]=3)[C:4]=2[NH2:5])[CH:14]=1

Komponenten

5

Versuchsvorschrift

3-chloro-2-(7-chloro-1,3-benzodioxol-5-yl)-4,4,4-trifluoro-but-2-enenitrile (20.2 g, 65.4 mmol) was dissolved in ethanol (200 mL) and treated with pyrimidin-2-yl-hydrazine (7.20 g, 65.4 mmol) and triethylamine (6.60 g, 65.4 mmol). The reaction mixture was heated to reflux for 10 h. The solvent was removed in vacuo, to the residue was added water, extracted with EtOAc, then the organic layer was combined, washed with water and brine, dried, filtered and concentrated to give crude product. The crude product was washed with DCM to give the title compound (11.0 g; 44%).

Aufarbeitung

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux for 10 h
  3. customThe solvent was removed in vacuo, to the residue
  4. additionwas added water
  5. extractionextracted with EtOAc
  6. washwashed with water and brine
  7. customdried
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customto give crude product
  11. washThe crude product was washed with DCM

Quellen und Nachweise

ORD-Eintrag
ord-ad6ad92f945645c5a0d9b2db56f7291b
Quelldatensatz
uspto-grants-2015_11
Patentnummer
US09174967B2

Verknüpfte Notizen

Wird geladen…