HCID 18689941, compound → HCID 15462193, compound
Reaction equation
Cl[CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:14]=[CH:13][C:12]([CH3:15])=[C:11]2[C:7]=1[C:8]([CH3:18])([CH3:17])[C:9](=[O:16])[NH:10]2.[N:19]1[C:28]2[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=2)[CH:22]=[CH:21][C:20]=1[CH2:29][CH:30]1[CH2:35][CH2:34][NH:33][CH2:32][CH2:31]1>>[N:19]1[C:28]2[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=2)[CH:22]=[CH:21][C:20]=1[CH2:29][CH:30]1[CH2:31][CH2:32][N:33]([CH2:2][CH2:3][CH2:4][O:5][C:6]2[CH:14]=[CH:13][C:12]([CH3:15])=[C:11]3[C:7]=2[C:8]([CH3:18])([CH3:17])[C:9](=[O:16])[NH:10]3)[CH2:34][CH2:35]1Participants
3
Procedure
In a manner similar to that described in Example 1, 4-(3-chloropropoxy)-3,3,7-trimethyl-2,3-dihydro-1H-indol-2-one (268 mg) and 4-(2-quinolylmethyl)piperidine (226 mg) were processed, to thereby obtain the title compound as white powder.
Sources & evidence
- ORD record
- ord-ac695ef8836d445a8e789d76fe57faa6
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06107308
Reaction notes
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