Hydrochloric Acid → methyl 2-oxo-2,3-dihydro-1H-1,3-benzodiazole-5-carboxylate

HRID 1365563Notes

Reaction equation

HRID 1365563 reaction equation
Cl.Cl.[NH2:3][C:4]1[CH:5]=[C:6]([CH:11]=[CH:12][C:13]=1[NH2:14])[C:7]([O:9][CH3:10])=[O:8].N[C:16](N)=[O:17].Cl>O>[O:17]=[C:16]1[NH:3][C:4]2[CH:5]=[C:6]([C:7]([O:9][CH3:10])=[O:8])[CH:11]=[CH:12][C:13]=2[NH:14]1

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 1176UreaHCID 18174510Methyl 3,4-diaminobenzoate dihydrochloride

Product 1

HCID 10352553methyl 2-oxo-2,3-dihydro-1H-1,3-benzodiazole-5-carboxylate

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Conditions

Temperature
150 °C

Procedure

Methyl 3,4-diaminobenzoate dihydrochloride (20 g, 0.08 mol) was mixed with urea (6.54 g, 0.11 mol). Reaction mixture was heated at ˜150° C. for 7 hours. After cooling powder was suspended in water (400 ml) and pH of the last one was adjusted to 0.45 with hydrochloric acid. Precipitate was filtered and rinsed with water and hydrochloric acid (pH=1.5). Obtained filter cake was dried at ˜100° C. Yield 15.7 g (97%).

Workup

  1. customReaction mixture
  2. temperatureAfter cooling powder
  3. filtrationPrecipitate was filtered
  4. washrinsed with water and hydrochloric acid (pH=1.5)
  5. customObtained
  6. filtrationfilter cake
  7. customwas dried at ˜100° C

Sources & evidence

ORD record
ord-8e0da6291ea8441591773de109c57f35
Source dataset
uspto-grants-2011_02
Patent number
US07889297B2

Reaction notes

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