1-Aminotetralin, (S)- → HCID 69721641, compound

HRID 2307662Notes

Reaction equation

HRID 2307662 reaction equation
[CH:1]([C:3]1[CH:4]=[C:5]([CH:15]=[CH:16][CH:17]=1)[O:6][C:7]1[CH:14]=[CH:13][C:10]([C:11]#[N:12])=[CH:9][CH:8]=1)=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>>[C@@H:18]1([NH:28][CH2:1][C:3]2[CH:4]=[C:5]([CH:15]=[CH:16][CH:17]=2)[O:6][C:7]2[CH:14]=[CH:13][C:10]([C:11]#[N:12])=[CH:9][CH:8]=2)[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 70580741-Aminotetralin, (S)-HCID 132385404-(3-Formylphenoxy)benzonitrile

Product 1

HCID 69721641HCID 69721641, compound

Procedure

The product from Example 50A 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-c063d0773a544963ba255f117533dccf
Source dataset
uspto-grants-2004_12
Patent number
US06831193B2

Reaction notes

Loading…