methyl 5-(4-((3-nitrophenyl)amino)pyridin-2-yl)-1H-pyrrole-3-carboxylate → methyl 5-(4-((3-aminophenyl)amino)pyridin-2-yl)-1H-pyrrole-3-carboxylate

HRID 1915048ノート

反応式

HRID 1915048 の反応式
[N+:1]([C:4]1[CH:5]=[C:6]([NH:10][C:11]2[CH:16]=[CH:15][N:14]=[C:13]([C:17]3[NH:21][CH:20]=[C:19]([C:22]([O:24][CH3:25])=[O:23])[CH:18]=3)[CH:12]=2)[CH:7]=[CH:8][CH:9]=1)([O-])=O>CCOC(C)=O.CCO>[NH2:1][C:4]1[CH:5]=[C:6]([NH:10][C:11]2[CH:16]=[CH:15][N:14]=[C:13]([C:17]3[NH:21][CH:20]=[C:19]([C:22]([O:24][CH3:25])=[O:23])[CH:18]=3)[CH:12]=2)[CH:7]=[CH:8][CH:9]=1

参加物

3

実験手順

Methyl 5-(4-((3-nitrophenyl)amino)pyridin-2-yl)-1H-pyrrole-3-carboxylate (1.32 g, 3.9 mmol) was taken up in EtOAc/EtOH (1:1; 90 mL) and purged with N2. Pd/C (10%, 0.145 g) was added and the mixture was stirred under an atmosphere of H2 at rt for 18 h. The mixture was filtered over celite, washing with EtOAc/EtOH. The filtrate was concentrated, taken back up in EtOAc and filtered over celite again to remove any residual catalyst. The filtrate was concentrated again and taken back up in EtOAc. The solution was filtered and the filtrate was concentrated to afford a tan solid. The solid was washed with CH2Cl2/hexanes (1:2) and dried under high vacuum to afford methyl 5-(4-((3-aminophenyl)amino)pyridin-2-yl)-1H-pyrrole-3-carboxylate (1.15 g, 96% yield) as a tan solid.

後処理

  1. custompurged with N2
  2. additionPd/C (10%, 0.145 g) was added
  3. filtrationThe mixture was filtered over celite
  4. washwashing with EtOAc/EtOH
  5. concentrationThe filtrate was concentrated
  6. filtrationfiltered over celite again
  7. customto remove any residual catalyst
  8. concentrationThe filtrate was concentrated again
  9. filtrationThe solution was filtered
  10. concentrationthe filtrate was concentrated
  11. customto afford a tan solid
  12. washThe solid was washed with CH2Cl2/hexanes (1:2)
  13. customdried under high vacuum

出典と根拠

ORDレコード
ord-3a8802fd73a84e9daee16077f80c571c
出典データセット
uspto-grants-2013_12
特許番号
US08614234B2

反応ノート

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