反応 #2328984

ord-f84ccbfe89c146a9bab2602423914949

反応方程式

ClCc1ccc(Cl)nc1
6-Chloronicotinyl chloride
COc1ccc(N)c(O)c1
2-hydroxy-4-methoxyaniline
CCN(CC)CC
triethylamine
C1CCOC1
THF
C1CCOC1
THF
COc1ccc(NC(=O)c2ccc(Cl)nc2)c(O)c1
title compound
COc1ccc(NC(=O)c2ccc(Cl)nc2)c(O)c1
6-Chloro-N-(2-hydroxy-4-methoxyphenyl)nicotinamide

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度was then heated
  2. 2
    温度to reflux for 5 minutes
  3. 3
    その他was collected
  4. 4
    洗浄rinsed with water
  5. 5
    乾燥dried (under vacuum over P2O5)

実験手順

6-Chloronicotinyl chloride (2.0 g, 11.4 mmol) in THF (10 mL) was added dropwise to a mixture of 2-hydroxy-4-methoxyaniline (1.58 g) and triethylamine (1.8 mL) in THF (20 mL) at r.t. The reaction was stirred at r.t for 30 minutes and was then heated to reflux for 5 minutes. After cooling to r.t. the solid was collected, rinsed with water, dried (under vacuum over P2O5), to give the title compound (1.77 g) as an orange solid. 1H NMR δ ppm 9.78 (br. s, 1H) 9.63 (br. s, 1H) 8.94 (d, 1H) 8.34 (dd, 1H) 7.68 (d, 1H) 7.34 (d, 1H) 6.49 (d, 1H) 6.42 (dd, 1H) 3.71 (s, 3H); MS m/z (M+H) 279, 281; (M−H) 277, 279.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07670591B2uspto-grants-2010_03