4-Nitrobenzoyl chloride → HCID 11573975, compound

HRID 1712038Notes

Reaction equation

HRID 1712038 reaction equation
[N+:1]([C:4]1[CH:12]=[CH:11][C:7]([C:8](Cl)=[O:9])=[CH:6][CH:5]=1)([O-:3])=[O:2].[CH3:13][O:14][C:15]1[CH:16]=[C:17]([C:21]2([OH:27])[CH2:26][CH2:25][CH2:24][NH:23][CH2:22]2)[CH:18]=[CH:19][CH:20]=1>>[OH:27][C:21]1([C:17]2[CH:18]=[CH:19][CH:20]=[C:15]([O:14][CH3:13])[CH:16]=2)[CH2:26][CH2:25][CH2:24][N:23]([C:8]([C:7]2[CH:11]=[CH:12][C:4]([N+:1]([O-:3])=[O:2])=[CH:5][CH:6]=2)=[O:9])[CH2:22]1

Participants

3

Reactant 2

HCID 85024-Nitrobenzoyl chlorideHCID 116516763-(3-Methoxy-phenyl)-piperidine-3-ol

Product 1

HCID 11573975HCID 11573975, compound

Procedure

The compound of Example 17 was prepared according to the general preparation protocol A from 4-nitrobenzoyl chloride and 3-(3-methoxy-phenyl)-piperidine-3-ol.

Sources & evidence

ORD record
ord-ac0259e530664ceabd9c88c7543da4f7
Source dataset
uspto-grants-2010_09
Patent number
US07790898B2

Reaction notes

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