3,5-Dimethoxybenzaldehyde → HCID 775447, compound

HRID 2307680Notes

Reaction equation

HRID 2307680 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[C:9]([O:11][CH3:12])[CH:10]=1)[CH:6]=O.[C@@H:13]1([NH2:23])[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH2:16][CH2:15][CH2:14]1>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[C:9]([O:11][CH3:12])[CH:10]=1)[CH2:6][NH:23][C@@H:13]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH2:16][CH2:15][CH2:14]1

Participants

3

Reactant 2

HCID 817473,5-DimethoxybenzaldehydeHCID 70580741-Aminotetralin, (S)-

Product 1

HCID 775447HCID 775447, compound

Procedure

3,5-Dimethoxybenzaldehyde 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-7afa154e8afe463bba65f4905956b0d5
Source dataset
uspto-grants-2004_12
Patent number
US06831193B2

Reaction notes

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