Ammonia → HCID 10360971, compound
Reaction equation
C[O:2][C:3](=O)[C:4]1[C:5](=[CH:10][C:11]([N:22]([CH3:29])[C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)=[C:12]([N:14]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH3:15])[CH:13]=1)[C:6]([O:8]C)=O.[NH3:31]>C(O)CO>[CH3:15][N:14]([C:12]1[CH:13]=[C:4]2[C:3](=[O:2])[NH:31][C:6](=[O:8])[C:5]2=[CH:10][C:11]=1[N:22]([C:23]1[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=1)[CH3:29])[C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Analogously to Example 1, 66 mg (0.16 mmol) of 4,5-bis(N-methyl-N-phenylamino)phthalic acid dimethyl ester (Example 14 A) in 5 ml of ethylene glycol are heated at 120° and, with stirring, ammonia gas is passed through the mixture for 18 hours. The reaction mixture is cooled, and extracted with ethyl acetate. The ethyl acetate phases are washed in succession three times with water and once with saturated sodium chloride solution, dried with sodium sulfate and concentrated by evaporation. The evaporation residue is chromatographed on silica gel with hexane/ethyl acetate 1:1 and the product fractions are combined and concentrated by evaporation, yielding the title compound in the form of slightly yellow crystals, FAB-MS: 358 [M+ +H], 1H-NMR (CDCl3): 3.05 (s, 6H).
Workup
- temperatureThe reaction mixture is cooled
- extractionextracted with ethyl acetate
- washThe ethyl acetate phases are washed in succession three times with water and once with saturated sodium chloride solution
- dry with materialdried with sodium sulfate
- concentrationconcentrated by evaporation
- customThe evaporation residue is chromatographed on silica gel with hexane/ethyl acetate 1:1
- concentrationconcentrated by evaporation
Sources & evidence
- ORD record
- ord-f79837030d4544cea14f3631cc70179d
- Source dataset
- uspto-grants-1997_09
- Patent number
- US05663336
Reaction notes
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