Sodium Carbonate → HCID 13067124, compound
Reaction equation
P(Cl)(Cl)(Cl)=O.[Cl:6][C:7]1[CH:28]=[CH:27][C:10]2[C:11]3[C:12](=[CH:23][NH:24][C:25]=3[CH3:26])[CH2:13][N:14]=[C:15]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=3[Cl:22])[C:9]=2[CH:8]=1.[C:29](=O)([O-])[O-:30].[Na+].[Na+]>CN(C)C=O>[Cl:6][C:7]1[CH:28]=[CH:27][C:10]2[C:11]3[C:12](=[C:23]([CH:29]=[O:30])[NH:24][C:25]=3[CH3:26])[CH2:13][N:14]=[C:15]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=3[Cl:22])[C:9]=2[CH:8]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
By means of a syringe 0.6 ml (6.5 mmol) of phosphorous oxychloride was added to a solution of 0.7 g (2.0 mmol) of 8-chloro-6-(2-chlorophenyl)-1-methyl-2H,4H-pyrrolo[3,4-d][2]benzazepine in 8 ml of dimethylformamide which was cooled to 0°. The mixture was stirred at 0° for 1 hr, poured into 50 ml of saturated aqueous sodium carbonate and extracted with methylene chloride. The methylene chloride solution was washed with water, dried over anhydrous sodium sulfate and concentrated at reduced pressure to give a red amorphous solid. Purification by column chromatography (silica gel, 20 g; 4% ether in methylene chloride, eluent) gave an off-white solid. Recrystallization from a mixture of methylene chloride and ethyl acetate gave off-white crystals, mp 274°-276°.
Workup
- temperaturewas cooled to 0°
- extractionextracted with methylene chloride
- washThe methylene chloride solution was washed with water
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated at reduced pressure
- customto give a red amorphous solid
- customPurification by column chromatography (silica gel, 20 g; 4% ether in methylene chloride, eluent)
- customgave an off-white solid
- customRecrystallization
- additionfrom a mixture of methylene chloride and ethyl acetate
- customgave off-white crystals, mp 274°-276°
Sources & evidence
- ORD record
- ord-467436fba4274dd8949c1aa435204653
- Source dataset
- uspto-grants-1983_09
- Patent number
- US04405518
Reaction notes
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