Ammonia → 6-(Trifluoromethyl)pyrimidin-4-amine

HRID 895143

Reaktionsgleichung

Reaktionsgleichung von HRID 895143
Cl[C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[N:5]=[CH:4][N:3]=1.FC(F)(F)C1N=C[N:17]=C(O)C=1.N>C(#N)C>[NH2:17][C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[N:5]=[CH:4][N:3]=1

Komponenten

5

Edukt 3

HCID 222AmmoniaHCID 115428814-Chloro-6-(trifluoromethyl)pyrimidineHCID 178516143HCID 178516143, Verbindung

Produkt 1

HCID 223857566-(Trifluoromethyl)pyrimidin-4-amineAusbeute 98 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

To a stirred mixture of 4-chloro-6-trifluoromethylpyrimidine (prepared from 6-trifluoromethyl-4-pyrimidinol as described in U.S. Pat. No. 5,714,438) (17.14 g, 93.9 mmol) in acetonitrile (282 ml) was added 25% aqueous ammonia solution (564 ml) and the mixture was stirred at room temperature for 23 h. The mixture was extracted with ethyl acetate (3×1 l), and the combined extracts were dried (MgSO4) and evaporated in vacuo to leave 14.97 g (98%) of the title compound as a white solid: 1H NMR (360 MHz, DMSO-d6) δ 6.80 (1H, s), 7.52 (2H, br s), 8.49 (1H, s).

Aufarbeitung

  1. extractionThe mixture was extracted with ethyl acetate (3×1 l)
  2. dry with materialthe combined extracts were dried (MgSO4)
  3. customevaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-0dca8a64aaf84101b3e1c3d483feb455
Quelldatensatz
uspto-grants-2005_07
Patentnummer
US06914065B2

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