Methylamine → 2,6-Dichloro-N-methylpyridin-4-amine

HRID 226209

反応式

HRID 226209 の反応式
[CH3:1][NH2:2].[Cl:3][C:4]1[CH:9]=[C:8](Cl)[CH:7]=[C:6]([Cl:11])[N:5]=1>C(O)C>[Cl:3][C:4]1[CH:9]=[C:8]([NH:2][CH3:1])[CH:7]=[C:6]([Cl:11])[N:5]=1

参加物

4

反応条件

温度
57.5 °C

実験手順

An 8M solution of methylamine in ethanol (5 ml; 40 mmol) was added drop wise to a stirred solution of 2,4,6-trichloropyridine (5 g; 27.4 mmol) in absolute ethanol (50 ml). After heating to 55-60° C. for 24 hr, the mixture was cooled to rt and concentrated. After adding water (50 ml) to the residue, the resulting suspension was filtered and the white filter cake was washed with water (3×10 ml). After air drying, the solid was suspended in dichloromethane (25 ml) and stirred for 10 minutes. Filtration, rinsing with dichloromethane and drying afforded 2.45 g (51%) of A1.6 as a white solid. HPLC (A): 95%, ret. time=1.16 min., LC/MS (M+H)+=177.00 (178.99).

後処理

  1. temperaturethe mixture was cooled to rt
  2. concentrationconcentrated
  3. additionAfter adding water (50 ml) to the residue
  4. filtrationthe resulting suspension was filtered
  5. washthe white filter cake was washed with water (3×10 ml)
  6. customAfter air drying
  7. filtrationFiltration
  8. washrinsing with dichloromethane
  9. customdrying
  10. customafforded 2.45 g (51%) of A1.6 as a white solid

出典と根拠

ORDレコード
ord-272212491dca4f0c92f071200cef1acb
出典データセット
uspto-grants-2009_07
特許番号
US07557211B2

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