HCID 11615419, compound → HCID 70391496, compound

HRID 1762376Notes

Reaction equation

HRID 1762376 reaction equation
[CH3:1][N:2]([CH3:15])[C:3]1[C:10]([O:11][CH3:12])=[CH:9][C:6]([CH:7]=O)=[CH:5][C:4]=1[O:13][CH3:14].[Cl-:16].[NH2:17][N+:18]1[CH:22]=[CH:21][N:20]([NH2:23])[C:19]=1[CH2:24][CH2:25][CH3:26]>C(O)(=O)C>[Cl-:16].[CH3:1][N:2]([CH3:15])[C:3]1[C:10]([O:11][CH3:12])=[CH:9][C:6]([CH:7]=[N:17][N+:18]2[CH:22]=[CH:21][N:20]([N:23]=[CH:7][C:6]3[CH:9]=[C:10]([O:11][CH3:12])[C:3]([N:2]([CH3:1])[CH3:15])=[C:4]([O:13][CH3:14])[CH:5]=3)[C:19]=2[CH2:24][CH2:25][CH3:26])=[CH:5][C:4]=1[O:13][CH3:14]

Participants

4

Procedure

1.43 g (6.8 mmol) of 4-dimethylamino-3,5-dimethoxy-benzaldehyde are added to a solution of 0.60 g (3.4 mmol) of 1,3-diamino-2-propyl-imidazolium chloride in 5 ml of glacial acetic acid. After leaving to stand for 16 hours the product is crystallized out by the addition of ether and then recrystallized from ethanol. There is obtained 1,3-bis[[4-(dimethylamino)-3,5-dimethoxybenzylidene]amino]-2-propylimidazolium chloride of melting point 218°-219°.

Workup

  1. customAfter leaving
  2. customthe product is crystallized out by the addition of ether
  3. customrecrystallized from ethanol

Sources & evidence

ORD record
ord-466dfaa8c74243f3a654146d72fb2059
Source dataset
uspto-grants-1989_05
Patent number
US04831151

Reaction notes

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