Potassium Iodide → 3-(4-Methoxybenzyl)-6-(methylamino)pyrimidin-4(3H)-one

HRID 2067738Notes

Reaction equation

HRID 2067738 reaction equation
[CH3:1][NH:2][C:3]1[N:8]=[CH:7][NH:6][C:5](=[O:9])[CH:4]=1.[CH3:10][O:11][C:12]1[CH:19]=[CH:18][C:15]([CH2:16]Cl)=[CH:14][CH:13]=1.[I-].[K+].C(=O)([O-])[O-].[Cs+].[Cs+]>CN(C=O)C>[CH3:10][O:11][C:12]1[CH:19]=[CH:18][C:15]([CH2:16][N:6]2[C:5](=[O:9])[CH:4]=[C:3]([NH:2][CH3:1])[N:8]=[CH:7]2)=[CH:14][CH:13]=1

Participants

6

Procedure

6-(Methylamino)pyrimidin-4(3H)-one (100 g, 800 mmol, 1 eq), p-methoxybenzyl chloride (124.8 g, 800 mmol, 1 eq), potassium iodide (13.3 g, 80 mmol, 0.1 eq) and cesium carbonate (260 g, 800 mmol, 1 eq) were stirred at RT in anhydrous DMF (1 L) for 8 hours. The DMF was removed in vacuo and the residue stirred overnight in 20% methanol/DCM. The solid was removed by filtration and washed with 20% methanol/DCM. The solvent was removed in vacuo and the resulting residue taken up in DCM then washed with water. The organic layer was dried over magnesium sulfate and evaporated to give 102 g of the title compound (59%). 1H NMR (400 MHz, DMSO-d6) δ ppm 2.63 (d, J=4.29 Hz, 3 H) 3.72 (s, 3 H) 4.87 (s, 2 H) 6.88 (d, J=8.84 Hz, 2 H) 7.25 (d, J=8.59 Hz, 2 H) 8.22 (s, 1 H). [M+H] calc'd for C13H15N3O2, 246; found, 246.

Workup

  1. customThe DMF was removed in vacuo
  2. customThe solid was removed by filtration
  3. washwashed with 20% methanol/DCM
  4. customThe solvent was removed in vacuo
  5. washthen washed with water
  6. dry with materialThe organic layer was dried over magnesium sulfate
  7. customevaporated

Sources & evidence

ORD record
ord-ca55730ff57f4a01a9c555a8066162b3
Source dataset
uspto-grants-2012_10
Patent number
US08293901B2

Reaction notes

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