Potassium Carbonate → 3-(5-Amino-3-tert-butyl-pyrazol-1-yl)-5-methyl-phenol

HRID 60644

反応式

HRID 60644 の反応式
[C:1]([C:5]1[CH:6]=[C:7]([NH2:10])[NH:8][N:9]=1)([CH3:4])([CH3:3])[CH3:2].C(=O)([O-])[O-].[K+].[K+].Br[C:18]1[CH:19]=[C:20]([OH:25])[CH:21]=[C:22]([CH3:24])[CH:23]=1.CN(C)[C@@H]1CCCC[C@H]1N>[Cu]I>[NH2:10][C:7]1[N:8]([C:18]2[CH:19]=[C:20]([OH:25])[CH:21]=[C:22]([CH3:24])[CH:23]=2)[N:9]=[C:5]([C:1]([CH3:4])([CH3:3])[CH3:2])[CH:6]=1

参加物

6

反応条件

温度
140 °C

実験手順

5-tert-Butyl-2H-pyrazol-3-ylamine (1.11 g, 8.00 mmol), potassium carbonate (2.32 g, 16.8 mmol), copper (I) iodide (0.076 g, 0.40 mmol), and 3-bromo-5-methylphenol (1.80 g, 9.60 mmol) were weighed into a large microwave vial. This was then purged with argon then trans-N,N-dimethylcyclohexane-1,2-diamine (0.25 mL, 1.60 mmol) added. To this mixture was then added degassed toluene (8 mL). The mixture was then purged with argon again, the vial sealed, and heated for 1 h at 140° C. in the microwave, then a further 4 h at 135° C. The mixture was cooled, diluted with ethyl acetate and passed through a pad of celite/silica, washing with more ethyl acetate. The dark solution was concentrated in vacuo. The residue was purified by FCC, using 0-40% DCM in EtOAc, to give the title compound (966 mg, 49%). 1H NMR (300 MHz, CDCl3): 1.32 (9H, s), 2.24 (3H, s), 3.82 (2H, br s), 5.49 (1H, s), 6.45-6.52 (1H, m), 6.65-6.71 (1H, m), 6.85-6.91 (1H, m).

後処理

  1. customThis was then purged with argon
  2. additionTo this mixture was then added
  3. customdegassed toluene (8 mL)
  4. customThe mixture was then purged with argon again
  5. customa further 4 h
  6. customat 135° C
  7. temperatureThe mixture was cooled
  8. additiondiluted with ethyl acetate
  9. washwashing with more ethyl acetate
  10. concentrationThe dark solution was concentrated in vacuo
  11. customThe residue was purified by FCC

出典と根拠

ORDレコード
ord-edfc02741a3e4efc8d0edf36bb885728
出典データセット
uspto-grants-2016_09
特許番号
US09440974B2

関連ノート

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