Water → 5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carbonitrile

HRID 1447378Notes

Reaction equation

HRID 1447378 reaction equation
[CH3:1][N:2]1[C:8](=[O:9])[C:7]2[CH:10]=[CH:11][CH:12]=[CH:13][C:6]=2[N:5]2[CH:14]=[N:15][C:16]([C:17]([NH2:19])=O)=[C:4]2[CH2:3]1.O.[OH-].[Na+]>C1(C)C=CC=CC=1>[CH3:1][N:2]1[C:8](=[O:9])[C:7]2[CH:10]=[CH:11][CH:12]=[CH:13][C:6]=2[N:5]2[CH:14]=[N:15][C:16]([C:17]#[N:19])=[C:4]2[CH2:3]1

Participants

5

Reactant 3

HCID 962WaterHCID 14798Sodium HydroxideHCID 20515321HCID 20515321, compound

Product 1

HCID 139845425-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carbonitrile

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

0.5 g of 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxamide is heated to reflux while stirring for 40 hours together with 0.5 g of Sicapent in 150 ml of toluene. The mixture is treated with a 0.5 g portion of Sicapent after 16 hours, 19 hours and 24 hours. The mixture is subsequently cooled and treated with water. The mixture is adjusted to pH 9 with 28 percent sodium hydroxide. After separation of the organic phase, the alkaline-aqueous phase is extracted twice with 250 ml of ethyl acetate each time. The organic extracts are washed twice with saturated sodium chloride solution, dried and evaporated. After crystallisation of the residue from methylene chloride/hexane, there is recovered a portion of unreacted starting material. The mother liquor is evaporated and chromatographed on 100 g of silica gel while eluting with ethyl acetate and alcohol. After recrystallisation of the thus-obtained substance from acetone, there is obtained 5,6-dihydro-5-methyl-6-oxo-4 H-imidazo[1,5-a][1,4]benzodiazepine-3-carbonitrile of melting point 184°-185° C.

Workup

  1. temperatureto reflux
  2. additionThe mixture is treated with a 0.5 g portion of Sicapent after 16 hours, 19 hours and 24 hours
  3. temperatureThe mixture is subsequently cooled
  4. customAfter separation of the organic phase
  5. extractionthe alkaline-aqueous phase is extracted twice with 250 ml of ethyl acetate each time
  6. washThe organic extracts are washed twice with saturated sodium chloride solution
  7. customdried
  8. customevaporated
  9. customAfter crystallisation of the residue from methylene chloride/hexane, there
  10. customis recovered a portion
  11. customThe mother liquor is evaporated
  12. customchromatographed on 100 g of silica gel
  13. washwhile eluting with ethyl acetate and alcohol
  14. customAfter recrystallisation of the thus-obtained substance from acetone

Sources & evidence

ORD record
ord-4fa05f32b80e472b928fec8c4d544dd0
Source dataset
uspto-grants-1982_02
Patent number
US04316839

Reaction notes

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