6-Methoxy-2-naphthol → 6-Methoxy-1-[(2-methoxyphenyl)-piperidin-1-yl-methyl]-naphthalen-2-ol

HRID 1270125Notes

Reaction equation

HRID 1270125 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([OH:13])[CH:7]=[CH:6]2.[Cl-].[CH3:15][O:16][C:17]1[CH:29]=[CH:28][CH:27]=[CH:26][C:18]=1[CH:19]=[N+:20]1[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]1>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[C:9]([CH:19]([C:18]1[CH:26]=[CH:27][CH:28]=[CH:29][C:17]=1[O:16][CH3:15])[N:20]1[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]1)=[C:8]([OH:13])[CH:7]=[CH:6]2

Participants

3

Procedure

The preparation was carried out in accordance with general synthesis instructions 4 from 6-methoxy-2-naphthol and 1-(2-methoxy-benzylidene)-piperidinium chloride, which had been prepared in accordance with example 32.

Workup

  1. customhad been prepared in accordance with example 32

Sources & evidence

ORD record
ord-481d9543e09e426da2b469a3977494f5
Source dataset
uspto-grants-2007_04
Patent number
US07202242B2

Reaction notes

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