Potassium Iodide → HCID 12614468, compound
Reaction equation
Br[CH2:2][CH2:3][S:4][CH:5]1[C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=2[O:9][C:8]2[CH:16]=[CH:17][CH:18]=[CH:19][C:7]=2[CH2:6]1.[NH:20]1[CH2:25][CH2:24][O:23][CH2:22][CH2:21]1.[C:26](=[O:29])([OH:28])[O-].[Na+].[I-].[K+]>CN(C)C=O.O>[C:10]([OH:9])(=[O:23])[C:26]([OH:28])=[O:29].[O:23]1[CH2:24][CH2:25][N:20]([CH2:2][CH2:3][S:4][CH:5]2[C:11]3[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=3[O:9][C:8]3[CH:16]=[CH:17][CH:18]=[CH:19][C:7]=3[CH2:6]2)[CH2:21][CH2:22]1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of 1.5 g of 10-(β-bromoethylthio)-10,11-dihydrodibenz[b,f]oxepin, Example 3, 0.5 g of morpholine, 1.0 g of sodium bicarbonate and 1.0 g of potassium iodide in 15 ml of dimethylformamide is stirred at 60°-70° C. for 64 hours. The reaction mixture is permitted to cool before being diluted with water. The biphasic mixture is extracted with ether and the combined ether extracts are shaken with a large excess of 2N hydrochloric acid. The acid solution is basified with potassium carbonate liberating the amine as an oil which is extracted into ether. The ethereal solution is dried and the ether is removed under vacuum regenerating an oil which is converted to its oxalate. The salt is recrystallized from a methanol-acetone-ether mixture to give colorless plates, mp 196°-198° C. of 10,11-dihydro-10-(β-morpholinoethylthio)dibenz[b,f]oxepin oxalate.
Workup
- temperatureto cool
- extractionThe biphasic mixture is extracted with ether
- stirringthe combined ether extracts are shaken with a large excess of 2N hydrochloric acid
- extractionis extracted into ether
- customThe ethereal solution is dried
- customthe ether is removed under vacuum
- customThe salt is recrystallized from a methanol-acetone-ether mixture
Sources & evidence
- ORD record
- ord-28f8e3fbc29b4100b739cc526ebfe5d7
- Source dataset
- uspto-grants-1989_06
- Patent number
- US04837227
Reaction notes
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