Potassium Carbonate → HCID 13689404, compound
Reaction equation
[NH:1]1[CH2:6][CH2:5][CH:4]([CH:7]2[C:13]3=[CH:14][CH:15]=[CH:16][N:12]3[CH2:11][C:10]3[CH:17]=[CH:18][CH:19]=[CH:20][C:9]=3[O:8]2)[CH2:3][CH2:2]1.[Cl:21][C:22]1[CH:23]=[C:24]([CH:28]=[CH:29][CH:30]=1)[CH2:25][CH2:26]Cl.C([O-])([O-])=O.[K+].[K+]>C(OCCCC)(=O)C>[Cl:21][C:22]1[CH:23]=[C:24]([CH2:25][CH2:26][N:1]2[CH2:2][CH2:3][CH:4]([CH:7]3[C:13]4=[CH:14][CH:15]=[CH:16][N:12]4[CH2:11][C:10]4[CH:17]=[CH:18][CH:19]=[CH:20][C:9]=4[O:8]3)[CH2:5][CH2:6]2)[CH:28]=[CH:29][CH:30]=1Participants
5
Procedure
A mixture of 11-(piperidin-4-yl)-5H,11H-pyrrolo[2,1-c][1,4]benzoxazepine (6.05 g, 0.023 mole), 3-chlorophenethyl chloride (4.74 g, 0.027 mole), K2CO3 (10.9 g) and KI (0.1 g) in 130 ml n-butyl acetate was refluxed for 50 hours. The reaction mixture was cooled, filtered and concentrated to an oil.
Workup
- temperaturewas refluxed for 50 hours
- temperatureThe reaction mixture was cooled
- filtrationfiltered
- concentrationconcentrated to an oil
Sources & evidence
- ORD record
- ord-b454e47a51664ad6af4526075bdbc85f
- Source dataset
- uspto-grants-1987_07
- Patent number
- US04681879
Reaction notes
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