HCID 67271832, compound → HCID 67272913, compound

HRID 1698535Notes

Reaction equation

HRID 1698535 reaction equation
[CH3:1][CH2:2][CH:3]([C:7]1[C:12]2[N:13]([CH3:17])[C:14](=O)[NH:15][C:11]=2[CH:10]=[CH:9][N:8]=1)[CH2:4][CH2:5][CH3:6].[Cl:18]C1N(C)C2C(C(CCC)CCC)=CC=CC=2N=1>>[Cl:18][C:14]1[N:13]([CH3:17])[C:12]2[C:7]([CH:3]([CH2:4][CH2:5][CH3:6])[CH2:2][CH3:1])=[N:8][CH:9]=[CH:10][C:11]=2[N:15]=1

Participants

3

Reactant 2

HCID 67271832HCID 67271832, compoundHCID 67272996HCID 67272996, compound

Product 1

HCID 67272913HCID 67272913, compound

Procedure

Prepared from 4-(hexan-3-yl)-3-methyl-1H-imidazo[4,5-c]pyridin-2(3H)-one according to the method described previously for 2-chloro-1-methyl-7-(1-propylbutyl)-1H-benzimidazole in 68% isolated yield.

Workup

  1. customisolated
  2. customyield

Sources & evidence

ORD record
ord-d5844c08f95e4c80b5ff2166a354b9d0
Source dataset
uspto-grants-2012_04
Patent number
US08163935B2

Reaction notes

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