3-(3,5-Dichlorophenoxy)benzaldehyde → HCID 69722316, compound

HRID 2307656Notes

Reaction equation

HRID 2307656 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:14]=[C:15]([Cl:17])[CH:16]=1)[O:5][C:6]1[CH:7]=[C:8]([CH:11]=[CH:12][CH:13]=1)[CH:9]=O.[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>>[Cl:1][C:2]1[CH:3]=[C:4]([CH:14]=[C:15]([Cl:17])[CH:16]=1)[O:5][C:6]1[CH:7]=[C:8]([CH:11]=[CH:12][CH:13]=1)[CH2:9][NH:28][C@@H:18]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[CH2:21][CH2:20][CH2:19]1

Participants

3

Reactant 2

HCID 6880503-(3,5-Dichlorophenoxy)benzaldehydeHCID 70580741-Aminotetralin, (S)-

Product 1

HCID 69722316HCID 69722316, compound

Procedure

3-(3,5-Dichlorophenoxy)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-6643ed70248d45599e04589058d44567
Source dataset
uspto-grants-2004_12
Patent number
US06831193B2

Reaction notes

Loading…