2-Amino-2,3-dimethylbutyronitrile → HCID 59301772, compound

HRID 2236350Notes

Reaction equation

HRID 2236350 reaction equation
[C:1]([C:3]([NH2:8])([CH3:7])[CH:4]([CH3:6])[CH3:5])#[N:2].[CH2:9]([O:12][C:13]1[C:21]([O:22][CH3:23])=[CH:20][C:16]([C:17](Cl)=[O:18])=[CH:15][C:14]=1[O:24][CH3:25])[C:10]#[CH:11]>>[C:1]([C:3]([NH:8][C:17](=[O:18])[C:16]1[CH:15]=[C:14]([O:24][CH3:25])[C:13]([O:12][CH2:9][C:10]#[CH:11])=[C:21]([O:22][CH3:23])[CH:20]=1)([CH3:7])[CH:4]([CH3:6])[CH3:5])#[N:2]

Participants

3

Reactant 2

HCID 943552-Amino-2,3-dimethylbutyronitrileHCID 574456693,5-Dimethoxy-4-(2-propynyloxy)benzoyl chloride

Product 1

HCID 59301772HCID 59301772, compound

Procedure

According to the same method as that of Production Example 1, 1-cyano-1,2-dimethylpropylamine was used in place of 2,2-dimethylpropylamine, 4-(2-propynyloxy)-3,5-dimethoxybenzoyl chloride was used in place of 4-(2-propynyloxy)-3-methoxybenzoyl chloride to obtain N-(1-cyano-1,2-dimethylpropyl)-4-(2-propynyloxy)-3,5-dimethoxybenzamide (hereinafter, described as the compound 19 of the present invention) represented by the formula:

Sources & evidence

ORD record
ord-7ececc2b98ac48a08cb3cb48a03ffb01
Source dataset
uspto-grants-2010_05
Patent number
US07714168B2

Reaction notes

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