Isoamylamine → HCID 59401399, compound

HRID 2060891Notes

Reaction equation

HRID 2060891 reaction equation
[CH:1]([C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6]([O:13][C:14]2[CH:21]=[CH:20][C:17]([C:18]#[N:19])=[CH:16][CH:15]=2)=[CH:5][CH:4]=1)=O.[CH3:22][CH:23]([CH3:27])[CH2:24][CH2:25][NH2:26]>>[CH3:22][CH:23]([CH3:27])[CH2:24][CH2:25][NH:26][CH2:1][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6]([O:13][C:14]2[CH:21]=[CH:20][C:17]([C:18]#[N:19])=[CH:16][CH:15]=2)=[CH:5][CH:4]=1

Participants

3

Reactant 2

HCID 7894IsoamylamineHCID 59401345HCID 59401345, compound

Product 1

HCID 59401399HCID 59401399, compound

Procedure

Using the procedure outlined in Example 1, 4-(4-formylnaphthalen-1-yloxy)benzonitrile (Preparation 28) and 3-methylbutylamine were converted to the title compound: RT=2.88 min; m/z (ES+)=345.3 [M+H]+.

Sources & evidence

ORD record
ord-730f797685224a11a533ae79787da58b
Source dataset
uspto-grants-2012_10
Patent number
US08278442B2

Reaction notes

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