2-Methoxybenzoic acid → 2-(Methyloxy)-n[1-(3-{[4-(methyloxy)phenyl]amino}-1,2,4-triazin-6-yl)ethyl]benzamide

HRID 2374974Notes

Reaction equation

HRID 2374974 reaction equation
COC1C=CC(NC2N=NC(C(NC(C3CCOCC3)=O)C)=CN=2)=CC=1.[NH2:27][CH:28]([C:30]1[N:35]=[N:34][C:33]([NH:36][C:37]2[CH:42]=[CH:41][C:40]([O:43][CH3:44])=[CH:39][CH:38]=2)=[N:32][CH:31]=1)[CH3:29].[CH3:45][O:46][C:47]1[CH:55]=[CH:54][CH:53]=[CH:52][C:48]=1[C:49](O)=[O:50]>>[CH3:45][O:46][C:47]1[CH:55]=[CH:54][CH:53]=[CH:52][C:48]=1[C:49]([NH:27][CH:28]([C:30]1[N:35]=[N:34][C:33]([NH:36][C:37]2[CH:42]=[CH:41][C:40]([O:43][CH3:44])=[CH:39][CH:38]=2)=[N:32][CH:31]=1)[CH3:29])=[O:50]

Participants

4

Procedure

In a similar manner as described for Intermediate 50, using 6-(1-aminoethyl)-N-[4-(methyloxy)phenyl]-1,2,4-triazin-3-amine (Intermediate 47) (100 mg, 0.41 mmol), and 2-methoxybenzoic acid (68 mg, 0.45 mmol) to give 2-(methyloxy)-N-[1-(3-{[4-(methyloxy)phenyl]amino-}-1,2,4-triazin-6-yl)ethyl]benzamide (145 mg) as a yellow solid. MS m/z 380 (M+1).

Sources & evidence

ORD record
ord-f682a3d01c59434cb63df6bef69058b9
Source dataset
uspto-grants-2008_12
Patent number
US07462614B2

Reaction notes

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