Hydrazine hydrate (1:1) → 4-[3-(N-glycyl-N-methylamino)-2,6-dichlorobenzyloxy]-1,2-dimethyl-1H-benzimidazole

HRID 2287554Notes

Reaction equation

HRID 2287554 reaction equation
[Cl:1][C:2]1[C:20]([N:21]([C:23](=[O:36])[CH2:24][N:25]2C(=O)C3=CC=CC=C3C2=O)[CH3:22])=[CH:19][CH:18]=[C:17]([Cl:37])[C:3]=1[CH2:4][O:5][C:6]1[C:14]2[N:13]=[C:12]([CH3:15])[N:11]([CH3:16])[C:10]=2[CH:9]=[CH:8][CH:7]=1.O.NN>C(O)C>[NH2:25][CH2:24][C:23]([N:21]([C:20]1[C:2]([Cl:1])=[C:3]([C:17]([Cl:37])=[CH:18][CH:19]=1)[CH2:4][O:5][C:6]1[C:14]2[N:13]=[C:12]([CH3:15])[N:11]([CH3:16])[C:10]=2[CH:9]=[CH:8][CH:7]=1)[CH3:22])=[O:36]

Participants

4

Procedure

A mixture of 4-[2,6-dichloro-3-[N-(phthalimidoacetyl)-N-methylamino]benzyloxy]-1,2-dimethyl-1H-benzimidazole (405 mg), hydrazine monohydrate (75.4 mg) and ethanol (4.0 ml) was refluxed for 30 minutes. After cooling, the resulting precipitate was filtered off, and the filtrate was concentrated in vacuo to give 4-[3-(N-glycyl-N-methylamino)-2,6-dichlorobenzyloxy]-1,2-dimethyl-1H-benzimidazole (300 mg).

Workup

  1. temperaturewas refluxed for 30 minutes
  2. temperatureAfter cooling
  3. filtrationthe resulting precipitate was filtered off
  4. concentrationthe filtrate was concentrated in vacuo

Sources & evidence

ORD record
ord-f62e319f2b294b2eb32f5e557adfb120
Source dataset
uspto-grants-2000_07
Patent number
US06083961

Reaction notes

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