N-Chlorobetainyl chloride → 2-({(3Z)-3-[(3,5-dimethyl-1H-pyrrol-2-yl)methylidene]-2-oxo-2,3-dihydro-1H-indol-1-yl}methoxy)-N,N,N-trimethyl-2-oxoethanaminium chloride
Reaction equation
[Cl-].[Cl:2][C:3](=[O:9])[CH2:4][N+:5]([CH3:8])([CH3:7])[CH3:6].[CH3:10][C:11]1[CH:15]=[C:14]([CH3:16])[NH:13][C:12]=1/[CH:17]=[C:18]1\[C:19](=[O:29])[N:20]([CH2:27][OH:28])[C:21]2[C:26]\1=[CH:25][CH:24]=[CH:23][CH:22]=2>>[Cl-:2].[CH3:10][C:11]1[CH:15]=[C:14]([CH3:16])[NH:13][C:12]=1/[CH:17]=[C:18]1\[C:19](=[O:29])[N:20]([CH2:27][O:28][C:3](=[O:9])[CH2:4][N+:5]([CH3:8])([CH3:7])[CH3:6])[C:21]2[C:26]\1=[CH:25][CH:24]=[CH:23][CH:22]=2Participants
3
Procedure
Following the procedure of Example 2, the title compound was prepared from 2-chloro-N,N,N-trimethyl-2-oxoethanaminium chloride and (3Z)-3-[(3,5-dimethyl-1H-pyrrol-2-yl)-methylidene]-1-(hydroxymethyl)-1,3-dihydro-2H-indol-2-one (1).
Sources & evidence
- ORD record
- ord-496334be1dcf46aa81a13f8fc57ac250
- Source dataset
- uspto-grants-2002_11
- Patent number
- US06482848B2
Reaction notes
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