2-Methylbenzaldehyde → HCID 10457986, compound

HRID 1179333Notes

Reaction equation

HRID 1179333 reaction equation
[Br:1][C:2]1[CH:23]=[CH:22][C:5]2[N:6]([CH:10]3[CH2:15][CH2:14][N:13]([CH:16]4[CH2:21][CH2:20][NH:19][CH2:18][CH2:17]4)[CH2:12][CH2:11]3)[C:7](=[O:9])[NH:8][C:4]=2[CH:3]=1.[CH3:24][C:25]1[CH:32]=[CH:31][CH:30]=[CH:29][C:26]=1[CH:27]=O>>[Br:1][C:2]1[CH:23]=[CH:22][C:5]2[N:6]([CH:10]3[CH2:15][CH2:14][N:13]([CH:16]4[CH2:17][CH2:18][N:19]([CH2:24][C:25]5[CH:32]=[CH:31][CH:30]=[CH:29][C:26]=5[CH3:27])[CH2:20][CH2:21]4)[CH2:12][CH2:11]3)[C:7](=[O:9])[NH:8][C:4]=2[CH:3]=1

Participants

3

Reactant 2

HCID 107222-MethylbenzaldehydeHCID 69458250HCID 69458250, compound

Product 1

HCID 10457986HCID 10457986, compound

Procedure

The title compound was prepared according to the procedure described in Example 18, using 5-bromo-1-[1-(piperidin-4-yl)piperidin-4-yl]-1,3-dihydro-2-H-benzimidazol-2one and 2-methylbenzaldehyde.

Sources & evidence

ORD record
ord-936b95febac4419cb0a754de1a2d93ca
Source dataset
uspto-grants-2007_10
Patent number
US07279490B2

Reaction notes

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