3-Phenylbenzaldehyde → HCID 69971069, compound

HRID 2307642Notes

Reaction equation

HRID 2307642 reaction equation
[C:1]1([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH:6]=[CH:5][CH:4]=[C:3]([CH:7]=O)[CH:2]=1.[C@@H:15]1([NH2:25])[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH2:18][CH2:17][CH2:16]1>>[C:1]1([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][NH:25][C@@H:15]2[C:24]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[CH2:18][CH2:17][CH2:16]2)[CH:2]=1

Participants

3

Reactant 2

HCID 1210533-PhenylbenzaldehydeHCID 70580741-Aminotetralin, (S)-

Product 1

HCID 69971069HCID 69971069, compound

Procedure

[1,1′-Biphenyl]-3-carbaldehyde 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-de5c167e19a643c8a61d485a99832714
Source dataset
uspto-grants-2004_12
Patent number
US06831193B2

Reaction notes

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