Nitrogen → 1-Methyl-3-{N-[beta-(4-hydroxyphenyl)ethyl]}carbamoyl-1,4-dihydropyridine

HRID 1719484Notes

Reaction equation

HRID 1719484 reaction equation
[I-].[CH3:2][N+:3]1[CH:8]=[CH:7][CH:6]=[C:5]([C:9](=[O:20])[NH:10][CH2:11][CH2:12][C:13]2[CH:18]=[CH:17][C:16]([OH:19])=[CH:15][CH:14]=2)[CH:4]=1.C(=O)(O)[O-].[Na+].N#N.S(S([O-])=O)([O-])=O.[Na+].[Na+]>O>[CH3:2][N:3]1[CH:8]=[CH:7][CH2:6][C:5]([C:9](=[O:20])[NH:10][CH2:11][CH2:12][C:13]2[CH:18]=[CH:17][C:16]([OH:19])=[CH:15][CH:14]=2)=[CH:4]1

Participants

6

Reactant 4

HCID 947NitrogenHCID 24489Sodium DithioniteHCID 516892Sodium BicarbonateHCID 134734281-Methyl-3-{N-[beta-(4-hydroxyphenyl)ethyl]}carbamoylpyridinium iodide

Product 1

HCID 147506161-Methyl-3-{N-[beta-(4-hydroxyphenyl)ethyl]}carbamoyl-1,4-dihydropyridine

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

To an ice cold solution of 1.15 g (3 mmol) of the product of Example 27 in 200 ml of deaerated water, 1.5 g (18 mmol) sodium bicarbonate were added. While the mixture was bubbled with N2 gas, 2.09 g (12 mmol) of sodium dithionite were gradually added to the mixture. The mixture was stirred under N2 for 1 hr and then extracted twice, each with 100 ml of ethyl acetate. The combined extract was washed with water, dried over anhydrous Na2SO4 and distilled on rotovap. Yield, 0.38 g (50%) of yellowish semisolid which reduced alcoholic AgNO3TS instantaneously. (PMR as expected.)

Workup

  1. additionwere gradually added to the mixture
  2. extractionextracted twice
  3. extractionThe combined extract
  4. washwas washed with water
  5. dry with materialdried over anhydrous Na2SO4
  6. distillationdistilled on rotovap
  7. customYield

Sources & evidence

ORD record
ord-5df6fb8cf54d479e9fb58fc8e82dd2f8
Source dataset
uspto-grants-1985_09
Patent number
US04540564

Reaction notes

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