1-(2,6-difluoro-4-nitrophenyl)-3-methyl-1H-1,2,4-triazole → 3,5-difluoro-4-(3-methyl-1H-1,2,4-triazol-1-yl)aniline

HRID 1803171ノート

反応式

HRID 1803171 の反応式
[F:1][C:2]1[CH:7]=[C:6]([N+:8]([O-])=O)[CH:5]=[C:4]([F:11])[C:3]=1[N:12]1[CH:16]=[N:15][C:14]([CH3:17])=[N:13]1>[Pd].CO>[F:1][C:2]1[CH:7]=[C:6]([CH:5]=[C:4]([F:11])[C:3]=1[N:12]1[CH:16]=[N:15][C:14]([CH3:17])=[N:13]1)[NH2:8]

参加物

4

実験手順

Step R (2): 10% Palladium on carbon (0.890 g, 0.830 mmol) was added under an atmosphere of nitrogen to a chilled (ice-water bath) solution of 1-(2,6-difluoro-4-nitrophenyl)-3-methyl-1H-1,2,4-triazole (2.00 g, 8.33 mmol dissolved in methanol (200 mL). The flask was repeatedly evacuated and flushed with hydrogen gas (double balloon). The resulting mixture was allowed to warm to rt and left to stir for 18 h under the hydrogen atmosphere. The vessel was subsequently purged with nitrogen gas. The crude reaction mixture was filtered through a short plug of diatomaceous earth (Celite®). The reaction vessel and Celite® were rinsed with fresh methanol. The combined filtrates were concentrated in vacuo. The residue was dried under high vacuum to afford 3,5-difluoro-4-(3-methyl-1H-1,2,4-triazol-1-yl)aniline (1.76 g, 8.37 mmol, quantitative yield) as a blackish/gray solid. LC-MS (M+H)+ 211.1. 1H NMR (500 MHz, CHLOROFORM-d) δ ppm 8.10 (1 H, s), 6.25-6.36 (2 H, m), 4.17 (2 H, br. s.), 2.49 (3 H, s).

後処理

  1. customThe flask was repeatedly evacuated
  2. customflushed with hydrogen gas (double balloon)
  3. waitleft
  4. customThe vessel was subsequently purged with nitrogen gas
  5. customThe crude reaction mixture
  6. filtrationwas filtered through a short plug of diatomaceous earth (Celite®)
  7. washThe reaction vessel and Celite® were rinsed with fresh methanol
  8. concentrationThe combined filtrates were concentrated in vacuo
  9. customThe residue was dried under high vacuum

出典と根拠

ORDレコード
ord-d02f34b9905942baa0d93ef576481a05
出典データセット
uspto-grants-2013_01
特許番号
US08349880B2

反応ノート

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