Sodium Bicarbonate → HCID 22759449, compound

HRID 1704388Notes

Reaction equation

HRID 1704388 reaction equation
Br.[Br:2][CH2:3][CH2:4][NH:5][C:6]1[CH2:10][CH:9]([C:11]2[C:16]([Cl:17])=[CH:15][CH:14]=[CH:13][C:12]=2[Cl:18])[CH2:8][N:7]=1.C(=O)(O)[O-].[Na+]>C(O)(C)C>[BrH:2].[Cl:18][C:12]1[CH:13]=[CH:14][CH:15]=[C:16]([Cl:17])[C:11]=1[CH:9]1[CH2:8][N:7]2[CH2:3][CH2:4][N:5]=[C:6]2[CH2:10]1

Participants

4

Procedure

A stirred mixture of 2-β-bromoethylamino-4-(2,6-dichlorophenyl)-1-pyrroline hydrobromide (46.35 g.), anhydrous sodium bicarbonate (9.3 g.) and dry isopropanol (350 ml.) is heated under reflux for 4 hours with exclusion of moisture, the hot mixture is filtered and the solid residue is stirred and heated under reflux with dry isopropanol (350 ml.) for 1 hour. The hot mixture is filtered and the combined isopropanol filtrates are evaporated to dryness under reduced pressure. The residue is dissolved in boiling ethanol (200 ml.) and the solution is concentrated to 125 ml. and allowed to cool. The mixture is filtered and there is thus obtained as solid residue 6-(2,6-dichlorophenyl)-2,3,6,7-tetrahydro-5H-pyrrolo[1,2-a]imidazole hydrobromide, m.p. 297°-299° C.

Workup

  1. temperatureis heated
  2. temperatureunder reflux for 4 hours with exclusion of moisture
  3. filtrationthe hot mixture is filtered
  4. temperatureheated
  5. temperatureunder reflux with dry isopropanol (350 ml.) for 1 hour
  6. filtrationThe hot mixture is filtered
  7. customthe combined isopropanol filtrates are evaporated to dryness under reduced pressure
  8. dissolutionThe residue is dissolved
  9. concentrationthe solution is concentrated to 125 ml
  10. temperatureto cool
  11. filtrationThe mixture is filtered

Sources & evidence

ORD record
ord-8dcd6d1af41c49b2986384f52598e8b5
Source dataset
uspto-grants-1978_11
Patent number
US04126685

Reaction notes

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