Piperidine → HCID 22475015, compound

HRID 2103142Notes

Reaction equation

HRID 2103142 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:8]2([C:20]3[CH:25]=[CH:24][CH:23]=[C:22]([Cl:26])[CH:21]=3)[O:12][C:11]3[CH:13]=[CH:14][C:15]([C:17](O)=[O:18])=[CH:16][C:10]=3[O:9]2)[CH:5]=[CH:6][CH:7]=1.[NH:27]1[CH2:32][CH2:31][CH2:30][CH2:29][CH2:28]1>>[Cl:1][C:2]1[CH:3]=[C:4]([C:8]2([C:20]3[CH:25]=[CH:24][CH:23]=[C:22]([Cl:26])[CH:21]=3)[O:12][C:11]3[CH:13]=[CH:14][C:15]([C:17]([N:27]4[CH2:32][CH2:31][CH2:30][CH2:29][CH2:28]4)=[O:18])=[CH:16][C:10]=3[O:9]2)[CH:5]=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 8082PiperidineHCID 22475183HCID 22475183, compound

Product 1

HCID 22475015HCID 22475015, compound

Procedure

This compound was prepared from 2,2-bis-(3-chloro-phenyl)-benzo[1,3]dioxole-5-carboxylic acid and piperidine according to Example 269f; light yellow solid, mp.: 54° C.,

Sources & evidence

ORD record
ord-f094f45c8060466ea03bca5b15b50798
Source dataset
uspto-grants-2009_08
Patent number
US07576088B2

Reaction notes

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