Hydrochloric Acid → HCID 14535921, compound
Reaction equation
[H-].[Na+].[CH3:3][O:4][C:5]1[CH:21]=[CH:20][C:8]([C:9]([C:11]2[CH:19]=[CH:18][CH:17]=[C:16]3[C:12]=2[CH:13]=[CH:14][NH:15]3)=[O:10])=[CH:7][CH:6]=1.[Cl:22][CH2:23][CH2:24][N:25]1[CH2:30][CH2:29][O:28][CH2:27][CH2:26]1.Cl>CCCCCC.CN(C=O)C.COC(C)(C)C.C(=O)(O)[O-].[Na+].C(OCC)(=O)C.O>[ClH:22].[CH3:3][O:4][C:5]1[CH:6]=[CH:7][C:8]([C:9]([C:11]2[CH:19]=[CH:18][CH:17]=[C:16]3[C:12]=2[CH:13]=[CH:14][N:15]3[CH2:23][CH2:24][N:25]2[CH2:30][CH2:29][O:28][CH2:27][CH2:26]2)=[O:10])=[CH:20][CH:21]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 6
Procedure
To a stirred mixture of 3.5 g (0.0887 mole) of a 60% suspension of sodium hydride in hexane in 50 ml of DMF was added 18.1 g (0.0721 mole) of 4-(4-methoxybenzoyl)indole The mixture was then treated with a solution containing 0.18 mole of 4-(2-chloroethyl)morpholine in t-butyl methyl ether (prepared by extraction of the free base from a suspension of 35.5 g of the corresponding hydrochloride in saturated sodium bicarbonate). When addition was complete, the reaction mixture was heated under reflux for about twelve hours, treated with 1500 ml of water and extracted with 500 ml of ethyl acetate. The combined organic extracts, on drying and evaporation to dryness, afforded an oil which was dissolved in 250 ml of ethyl acetate and treated with 50 ml of ethereal hydrogen chloride. The material which separated was collected and recrystallized from ethanol to give 20.3 g of 4-(4-methoxybenzoyl)-1-[2-(4-morpholinyl)ethyl]-1H-indole hydrochloride, m.p. 177°-180 ° C.
Workup
- additionwas then treated with a solution
- additionWhen addition
- temperaturethe reaction mixture was heated
- temperatureunder reflux for about twelve hours
- extractionextracted with 500 ml of ethyl acetate
- customThe combined organic extracts, on drying
- customevaporation to dryness
- customafforded an oil which
- customThe material which separated
- customwas collected
- customrecrystallized from ethanol
Sources & evidence
- ORD record
- ord-3ecaa2073f304d5299eed132da26245b
- Source dataset
- uspto-grants-1989_10
- Patent number
- US04874761
Reaction notes
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