N-Methylisobutylamine → HCID 10131672, compound

HRID 1064669Notes

Reaction equation

HRID 1064669 reaction equation
CS(O[CH2:6][CH2:7][C:8]1[O:9][C:10]2[CH:16]=[CH:15][C:14]([C:17]3[CH:22]=[CH:21][C:20]([C:23]#[N:24])=[CH:19][CH:18]=3)=[CH:13][C:11]=2[CH:12]=1)(=O)=O.[CH2:25]([NH:29][CH3:30])[CH:26]([CH3:28])[CH3:27]>>[CH2:25]([N:29]([CH3:30])[CH2:6][CH2:7][C:8]1[O:9][C:10]2[CH:16]=[CH:15][C:14]([C:17]3[CH:22]=[CH:21][C:20]([C:23]#[N:24])=[CH:19][CH:18]=3)=[CH:13][C:11]=2[CH:12]=1)[CH:26]([CH3:28])[CH3:27]

Participants

3

Reactant 2

HCID 12249N-MethylisobutylamineHCID 113936782-[5-(4-cyanophenyl)-1-benzofuran-2-yl]ethyl Methanesulfonate

Product 1

HCID 10131672HCID 10131672, compound

Procedure

The product from Example 1C and isobutyl(methyl)amine were processed as described in Example 1D to provide the titled compound. MS (DCI) m/z 333 (M+H)+;

Sources & evidence

ORD record
ord-47df1f7fa2f54a62a00bdcb428eea0a5
Source dataset
uspto-grants-2005_11
Patent number
US06969730B2

Reaction notes

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