Dimethylamine → HCID 14373876, compound

HRID 1841824Notes

Reaction equation

HRID 1841824 reaction equation
[CH2:1]=O.[CH3:3][NH:4][CH3:5].S(=O)(=O)(O)O.[Cl:11][C:12]1[CH:13]=[C:14]2[C:18](=[CH:19][C:20]=1[Cl:21])[NH:17][CH:16]=[CH:15]2.[Cl-].[Na+]>CN(C=O)C.O>[CH3:3][N:4]([CH2:1][C:15]1[C:14]2[C:18](=[CH:19][C:20]([Cl:21])=[C:12]([Cl:11])[CH:13]=2)[NH:17][CH:16]=1)[CH3:5]

Participants

8

Conditions

Temperature
2.5 °C

Procedure

Next, 37% aqueous formaldehyde solution and DMF are added into a reactor. The reactor is cooled to 0-5° C. and 33% aqueous dimethylamine solution then is added slowly with stirring. Concentrated sulfuric acid is added slowly to the mixture while the temperature is maintained at below 10° C. The mixture is stirred for an additional 15 minutes and cooled to 0-5° C. A solution of 5,6-dichloroindole (C) in DMF is added slowly to the reactor and stirred for an additional hour at 0-5° C. The mixture is allowed to warm to room temperature and stirred for 24 hrs. The mixture is then added to a reactor containing a solution of industrial sodium chloride in water. Activated carbon next is added and the mixture stirred for 30 minutes. Upon filtration, the filtrate is adjusted to pH>12 with 20% aqueous sodium hydroxide solution. The precipitate is filtered, washed with water until pH=7-8, centrifuged, and dried to yield crude 5,6-dichlorogramine (D). Recrystallization in 70% ethanol produces the pure product with melting point of 150-154° C.

Workup

  1. temperatureis maintained at below 10° C
  2. stirringThe mixture is stirred for an additional 15 minutes
  3. temperaturecooled to 0-5° C
  4. stirringstirred for an additional hour at 0-5° C
  5. temperatureto warm to room temperature
  6. stirringstirred for 24 hrs
  7. additionThe mixture is then added to a reactor
  8. additionActivated carbon next is added
  9. stirringthe mixture stirred for 30 minutes
  10. filtrationUpon filtration
  11. filtrationThe precipitate is filtered
  12. washwashed with water until pH=7-8
  13. customcentrifuged, and dried

Sources & evidence

ORD record
ord-2bd0491eb6174344b9027a217e0fe7eb
Source dataset
uspto-grants-2015_02
Patent number
US08945397B2

Reaction notes

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