Piperidine → HCID 22475141, compound

HRID 2103150Notes

Reaction equation

HRID 2103150 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:9]2([C:21]3[CH:26]=[C:25]([Cl:27])[CH:24]=[C:23]([Cl: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:5]=[C:6]([Cl:8])[CH:7]=1.[NH:29]1[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]1>>[Cl:28][C:23]1[CH:22]=[C:21]([C:9]2([C:4]3[CH:3]=[C:2]([Cl:1])[CH:7]=[C:6]([Cl:8])[CH:5]=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:26]=[C:25]([Cl:27])[CH:24]=1

Participants

3

Reactant 2

HCID 8082PiperidineHCID 22475246HCID 22475246, compound

Product 1

HCID 22475141HCID 22475141, compound

Procedure

This compound was prepared from 2,2-bis-(3,5-dichloro-phenyl)-benzo[1,3]dioxole-5-carboxylic acid and piperidine according to Example 269f; waxy solid,

Sources & evidence

ORD record
ord-1f75d57c6243400db9d90fc8b3158c96
Source dataset
uspto-grants-2009_08
Patent number
US07576088B2

Reaction notes

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