Sodium Hydroxide → 4-[(6-Amino-1,2,3,4-tetrahydro-1-methyl-2,4-dioxo-3-pyrimidinyl)methyl]benzonitrile

HRID 1638333Notes

Reaction equation

HRID 1638333 reaction equation
Br[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]#[N:10])=[CH:5][CH:4]=1.[NH2:11][C:12]1[N:17]([CH3:18])[C:16](=[O:19])[NH:15][C:14](=[O:20])[CH:13]=1.[OH-].[Na+]>C(O)C>[NH2:11][C:12]1[N:17]([CH3:18])[C:16](=[O:19])[N:15]([CH2:2][C:3]2[CH:8]=[CH:7][C:6]([C:9]#[N:10])=[CH:5][CH:4]=2)[C:14](=[O:20])[CH:13]=1

Participants

5

Reactant 3

HCID 14798Sodium HydroxideHCID 755206-Amino-1-methyluracilHCID 869964-(Bromomethyl)benzonitrile

Product 1

HCID 151364174-[(6-Amino-1,2,3,4-tetrahydro-1-methyl-2,4-dioxo-3-pyrimidinyl)methyl]benzonitrileYield 12.2%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

α-Bromo-p-tolunitrile (5.41 g, 27.6 mmol) was added at once with stirring to a solution of 6-amino-1-methyluracil (V. Papesch and E. F. Schroeder. J. Org. Chem. (1951), 16, 1879) (3.90 g, 27.6 mmol) in 1:1 ethanol: 1 N sodium hydroxide (56 ml) at 42° C. After 1.75 hours. the mixture was cooled, filtered and washed with water. The resulting solid and second crop obtained by evaporation of the filtrate were combined (5.80 g) and partially purified by silica gel chromatography followed by repeated trituration with 1:2 methanol; ether to give crude 4-[(6-Amino-1,2,3,4-tetrahydro-1-methyl-2,4-dioxo-3-pyrimidinyl)methyl]benzonitrile (0.86 g), indentified by NMR.

Workup

  1. customat 42° C
  2. temperaturethe mixture was cooled
  3. filtrationfiltered
  4. washwashed with water
  5. customThe resulting solid and second crop obtained by evaporation of the filtrate
  6. custompartially purified by silica gel chromatography

Sources & evidence

ORD record
ord-4f1594a64c8c4b72873056ce667de767
Source dataset
uspto-grants-1989_11
Patent number
US04879296

Reaction notes

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