Phenol → HCID 20131119, compound

HRID 1788987Notes

Reaction equation

HRID 1788987 reaction equation
O.[NH2:2][C:3]1[C:12]2[C:7](=[CH:8][C:9]([O:15][CH3:16])=[C:10]([O:13][CH3:14])[CH:11]=2)[N:6]=[C:5]([N:17]2[CH2:22][CH2:21][N:20]([C:23]3[CH:28]=[CH:27][N:26]=[C:25]([Cl:29])[N:24]=3)[CH2:19][CH2:18]2)[CH:4]=1.NC1[C:40]2[C:35](=[CH:36][C:37](OC)=[C:38]([O:41]C)[CH:39]=2)N=C(N2CCN(C3C=CN=C([Cl:57])N=3)CC2)C=1.C1(O)C=CC=CC=1.C(=O)([O-])[O-].[K+].[K+].[I-].[K+]>CC(C)CC(=O)C.CO.C(Cl)Cl>[ClH:29].[ClH:57].[NH2:2][C:3]1[C:12]2[C:7](=[CH:8][C:9]([O:15][CH3:16])=[C:10]([O:13][CH3:14])[CH:11]=2)[N:6]=[C:5]([N:17]2[CH2:22][CH2:21][N:20]([C:23]3[CH:28]=[CH:27][N:26]=[C:25]([O:41][C:38]4[CH:39]=[CH:40][CH:35]=[CH:36][CH:37]=4)[N:24]=3)[CH2:19][CH2:18]2)[CH:4]=1

Participants

8

Reactant 4

HCID 996Phenol2×HCID 4875Potassium Iodide2×HCID 11430Potassium Carbonate2×HCID 88639602HCID 88639602, compound

Product 1

HCID 20131119HCID 20131119, compoundYield 125.3%

Reagents, catalysts & solvents 3

HCID 887MethanolSolventHCID 6344DichloromethaneSolventHCID 7909Methyl Isobutyl KetoneSolvent

Procedure

4-Amino-2-[4-(2-chloropyrimidin-4-yl)piperazin-1-yl]-6,7-dimethoxyquinoline hemihydrate (0.32 g), phenol (0.15 g), anhydrous potassium carbonate (0.22 g) and potassium iodide (catalytic trace) in 4-methyl-2-pentanone (125 ml) were stirred under reflux for 18 hours. Further portions of phenol, anhydrous potassium carbonate and potassium iodide were then added thrice at 8 hour intervals, followed by a final 18 hours refluxing. After cooling, methylene chloride (50 ml) and methanol (20 ml) were added and the reaction mixture filtered. The filtrate was evaported in vacuo and the residue dissolved in methylene chloride, washed with water, dried (MgSO4) and evaporated in vacuo. Chromatography on silica (Merck 9385, 40 g) eluting with methylene chloride/methanol (100:0→88:12) followed by treatment of the product with ethereal hydrogen chloride and recrystallisation from isopropanol gave 4-amino-6,7-dimethoxy-2-[4-(2-phenoxypyrimidin-4-yl)piperazin-1-yl]quinoline dihydrochloride (0.26 g), m.p. 199°-201° (d).

Workup

  1. temperatureunder reflux for 18 hours
  2. custom18 hours
  3. temperaturerefluxing
  4. temperatureAfter cooling
  5. filtrationthe reaction mixture filtered
  6. dissolutionthe residue dissolved in methylene chloride
  7. washwashed with water
  8. dry with materialdried (MgSO4)
  9. customevaporated in vacuo
  10. washChromatography on silica (Merck 9385, 40 g) eluting with methylene chloride/methanol (100:0→88:12)
  11. customfollowed by treatment of the product with ethereal hydrogen chloride and recrystallisation from isopropanol

Sources & evidence

ORD record
ord-af56137fa4ef4309b9ed79595c9f42c5
Source dataset
uspto-grants-1987_08
Patent number
US04686228

Reaction notes

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