Triethylamine → HCID 13329077, compound

HRID 1904301Notes

Reaction equation

HRID 1904301 reaction equation
[Cl-].[CH3:2][NH+:3]1[CH2:8][CH2:7][C:6]([C:9](=O)[NH2:10])=[CH:5][CH2:4]1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.BrBr.C(N(CC)CC)C>[OH-].[Na+].C(Cl)Cl>[CH3:2][N:3]1[CH2:8][CH2:7][C:6]([C:9]#[N:10])=[CH:5][CH2:4]1

Participants

7

Procedure

A solution of 1-methyl-4-carbamoyl-1,2,5,6-tetrahydropyridinium chloride (3.6 g;20.4 mmol) in sodium hydroxide (4N)(30 ml) was extracted with methylene chloride (3×50 ml). The combined extracts were dried, filtered, and evaporated to 50 ml. To the extract a solution of triphenylphosphine (15.7 g; 60 mmol), bromine (3.3 ml; 65 mmol) and triethylamine (11 ml) in methYIenechlorid (150 ml) was added. The reaction was stirred at room temperature for 20 hours and evaporated in vacuo. The residue was dissolved in water (50 ml) and washed with methylene chloride (3×75 ml). To the water-phase sodium hydroxide (4N) (30 ml) was added and the mixture was extracted with methylene chloride. The combined extracts were dried, filtered, and evaporated in vacuo to give the title compound.

Workup

  1. customThe combined extracts were dried
  2. filtrationfiltered
  3. customevaporated to 50 ml
  4. additionwas added
  5. customevaporated in vacuo
  6. dissolutionThe residue was dissolved in water (50 ml)
  7. washwashed with methylene chloride (3×75 ml)
  8. additionTo the water-phase sodium hydroxide (4N) (30 ml) was added
  9. extractionthe mixture was extracted with methylene chloride
  10. customThe combined extracts were dried
  11. filtrationfiltered
  12. customevaporated in vacuo

Sources & evidence

ORD record
ord-5dd66df98ba84e4ab2ab6fdacacdf643
Source dataset
uspto-grants-1989_06
Patent number
US04837241

Reaction notes

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