Methyl 3-oxovalerate → HCID 178436943, compound

HRID 1450417Notes

Reaction equation

HRID 1450417 reaction equation
S(O)(O)(=O)=O.[NH2:6][C:7]1[NH:8][CH:9]=[CH:10][N:11]=1.[CH3:12][CH2:13][C:14]([CH2:16][C:17](OC)=[O:18])=O>C(O)(=O)C>[CH2:13]([C:14]1[CH:16]=[C:17]([OH:18])[N:8]2[CH:9]=[CH:10][N:11]=[C:7]2[N:6]=1)[CH3:12]

Participants

4

Reactant 2

HCID 121699Methyl 3-oxovalerateHCID 135136Bis(2-amino-1H-imidazole) sulphate

Product 1

HCID 178436943HCID 178436943, compound

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Procedure

20.0 g (151.4 mmol) commercially available (Aldrich) 2-aminoimidazole sulfate and 19.7 g (151.4 mmol) methyl 3-oxo-n-valerate were heated with reflux in 27 ml acetic acid for 7 h. After cooling to room temperature remaining solids were removed by filtration, and the filtrate was diluted with water, neutralized with sodium hydroxide, and extracted with dichloromethane. The organic layer was dried over sodium sulfate, evaporated in vacuo, while the title compound crystallized in colorless crystals, which were filtered with suction, washed with hexane, and dried in vacuo,

Workup

  1. customwere removed by filtration
  2. additionthe filtrate was diluted with water
  3. extractionextracted with dichloromethane
  4. dry with materialThe organic layer was dried over sodium sulfate
  5. customevaporated in vacuo, while the title compound
  6. customcrystallized in colorless crystals, which
  7. filtrationwere filtered with suction
  8. washwashed with hexane
  9. customdried in vacuo

Sources & evidence

ORD record
ord-e06b56dc6cd344d4b1beea23121e2ca0
Source dataset
uspto-grants-1997_02
Patent number
US05602136

Reaction notes

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