Phosphorus oxychloride → 7-Chloro-2,5-dimethyl-3-(4-chloro-2,6-dimethylphenyl)-pyrazolo[1,5-a]pyrimidine

HRID 1016450ノート

反応式

HRID 1016450 の反応式
O[C:2]1[N:7]2[N:8]=[C:9]([CH3:20])[C:10]([C:11]3[C:16]([CH3:17])=[CH:15][C:14]([Cl:18])=[CH:13][C:12]=3[CH3:19])=[C:6]2[N:5]=[C:4]([CH3:21])[CH:3]=1.C([O-])(O)=O.[Na+].O=P(Cl)(Cl)[Cl:29]>C(Cl)Cl>[Cl:29][C:2]1[N:7]2[N:8]=[C:9]([CH3:20])[C:10]([C:11]3[C:16]([CH3:17])=[CH:15][C:14]([Cl:18])=[CH:13][C:12]=3[CH3:19])=[C:6]2[N:5]=[C:4]([CH3:21])[CH:3]=1

参加物

5

実験手順

Slurry 7-hydroxy-2,5-dimethyl-3-(4-chloro-2,6-dimethylphenyl)-pyrazolo[1,5-a] pyrimidine in 10 mL POCl3 and reflux at 130° C. under N2. After 2 h, monitoring by TLC (alcohol Rf=0.5, chloride Rf=1.0; EtOAc as eluent), quench the reaction carefully at ambient temperature by diluting with 50 mL CH2Cl2 and pouring slowlyj into non-stirring saturated NaHCO3. Adjust stirring speed to control rate of quenching of residual POCl3 and stir until gas evolution ceases. Separate the layers and extract the aqueous layer with CH2Cl2 (2×50 mL). Pool the organic layers and dry over Na2SO4. Filter and evaporate to yellow oil, which is used directly without further purification.

後処理

  1. custommonitoring by TLC (alcohol Rf=0.5, chloride Rf=1.0; EtOAc as eluent), quench
  2. customthe reaction carefully at ambient temperature
  3. customof quenching of residual POCl3
  4. stirringstir until gas evolution ceases
  5. customSeparate the layers
  6. extractionextract the aqueous layer with CH2Cl2 (2×50 mL)
  7. dry with materialPool the organic layers and dry over Na2SO4
  8. filtrationFilter
  9. customevaporate to yellow oil, which
  10. customis used directly without further purification

出典と根拠

ORDレコード
ord-4754ff3c9cf147669cc696281f6a2e6a
出典データセット
uspto-grants-2002_11
特許番号
US06476038B1

反応ノート

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