3-(4-Methoxyphenoxy)benzaldehyde → HCID 69723270, compound

HRID 2307651Notes

Reaction equation

HRID 2307651 reaction equation
[CH3:1][O:2][C:3]1[CH:17]=[CH:16][C:6]([O:7][C:8]2[CH:9]=[C:10]([CH:13]=[CH:14][CH:15]=2)[CH:11]=O)=[CH:5][CH:4]=1.[C@@H:18]1([NH2:28])[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[CH2:21][CH2:20][CH2:19]1>>[CH3:1][O:2][C:3]1[CH:17]=[CH:16][C:6]([O:7][C:8]2[CH:9]=[C:10]([CH:13]=[CH:14][CH:15]=2)[CH2:11][NH:28][C@@H:18]2[C:27]3[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=3)[CH2:21][CH2:20][CH2:19]2)=[CH:5][CH:4]=1

Participants

3

Reactant 2

HCID 1235533-(4-Methoxyphenoxy)benzaldehydeHCID 70580741-Aminotetralin, (S)-

Product 1

HCID 69723270HCID 69723270, compound

Procedure

3-(4-Methoxyphenoxy)benzaldehyde and (1S)-1,2,3,4-tetrahydro-1-naphthalenylamine were processed as described in Example 1A to provide the title compound.

Sources & evidence

ORD record
ord-69122d74f8fe46d3b82a39911e46fbc3
Source dataset
uspto-grants-2004_12
Patent number
US06831193B2

Reaction notes

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