5-Methylisatoic anhydride → 2-Amino-N-(3-imidazol-1-yl-butyl)-5-methyl-benzamide

HRID 580467Notes

Reaction equation

HRID 580467 reaction equation
[CH3:1][C:2]1[CH:13]=[C:6]2[C:7]([O:9]C(=O)[NH:11][C:5]2=[CH:4][CH:3]=1)=O.[N:14]1([CH:19]([CH3:23])[CH2:20][CH2:21][NH2:22])[CH:18]=[CH:17][N:16]=[CH:15]1>>[NH2:11][C:5]1[CH:4]=[CH:3][C:2]([CH3:1])=[CH:13][C:6]=1[C:7]([NH:22][CH2:21][CH2:20][CH:19]([N:14]1[CH:18]=[CH:17][N:16]=[CH:15]1)[CH3:23])=[O:9]

Participants

3

Reactant 2

HCID 2944785-Methylisatoic anhydrideHCID 139528623-(1H-Imidazol-1-yl)butan-1-amine

Product 1

HCID 139527642-Amino-N-(3-imidazol-1-yl-butyl)-5-methyl-benzamide

Procedure

When 5-methylisatoic anhydride was reacted with 3-(1H-imidazol-1-yl)butanamine by the procedure of Example 11, the above compound, mp 128°-130° C., was obtained.

Workup

  1. customthe above compound, mp 128°-130° C., was obtained

Sources & evidence

ORD record
ord-544d126b13c647e4a2933a5f08d16d2d
Source dataset
uspto-grants-1988_06
Patent number
US04753944

Reaction notes

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