Piperidine → HCID 22475089, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:9]2([C:21]3[CH:26]=[CH:25][CH:24]=[C:23]([O:27][CH3:28])[CH:22]=3)[O:13][C:12]3[CH:14]=[CH:15][C:16]([C:18]([OH:20])=O)=[CH:17][C:11]=3[O:10]2)[CH:6]=[CH:7][CH:8]=1.[NH:29]1[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]1>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:9]2([C:21]3[CH:26]=[CH:25][CH:24]=[C:23]([O:27][CH3:28])[CH:22]=3)[O:13][C:12]3[CH:14]=[CH:15][C:16]([C:18]([N:29]4[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]4)=[O:20])=[CH:17][C:11]=3[O:10]2)[CH:6]=[CH:7][CH:8]=1Participants
3
Procedure
This compound was prepared from 2,2-bis-(3-methoxy-phenyl)-benzo[1,3]dioxole-5-carboxylic acid and piperidine according to Example 269f; waxy solid, MS: m/e=446 ([M+H]+].
Sources & evidence
- ORD record
- ord-562ea4f7c51c4f9788191e9ed049e8ab
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07576088B2
Reaction notes
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