Hydrogen Peroxide → HCID 131710120, compound
Reaction equation
Cl.[Cl:2][C:3]1[C:9](=[O:10])[N:8]([CH2:11][CH2:12][N:13]([CH3:15])[CH3:14])[C:7]2[CH:16]=[CH:17][CH:18]=[CH:19][C:6]=2[S:5][C:4]=1[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.[OH:26]O>C(O)(=O)C>[ClH:2].[Cl:2][C:3]1[C:9](=[O:10])[N:8]([CH2:11][CH2:12][N:13]([CH3:15])[CH3:14])[C:7]2[CH:16]=[CH:17][CH:18]=[CH:19][C:6]=2[S:5](=[O:26])[C:4]=1[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
3-Chloro-5-[2-(dimethylamino)ethyl]-2-phenyl-1,5-benzothiazepin-4(5H)-one, hydrochloride (prepared as described in Example 1) is treated with one equivalent of hydrogen peroxide in dilute acetic acid, and allowed to stand for about 16 hours. Solvent removal yields the title compound.
Workup
- customSolvent removal
Sources & evidence
- ORD record
- ord-3a6f266433fd471485ffa9c6df3da035
- Source dataset
- uspto-grants-1976_04
- Patent number
- US03948889
Reaction notes
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