Sodium Hydroxide → HCID 54380946, compound

HRID 1815276Notes

Reaction equation

HRID 1815276 reaction equation
[CH:1]([C:3]1[NH:7][C:6]([CH3:8])=[C:5]([C:9]([OH:11])=O)[C:4]=1[CH3:12])=[O:2].F[P-](F)(F)(F)(F)F.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1.C(N(C(C)C)CC)(C)C.[CH3:49][N:50]([CH3:54])[CH2:51][CH2:52][NH2:53].[OH-].[Na+]>CN(C)C=O.[Cl-].[Na+].O.O>[CH3:49][N:50]([CH3:54])[CH2:51][CH2:52][NH:53][C:9]([C:5]1[C:4]([CH3:12])=[C:3]([CH:1]=[O:2])[NH:7][C:6]=1[CH3:8])=[O:11]

Participants

9

Reactant 5

HCID 14798Sodium HydroxideHCID 66053N,N-DimethylethylenediamineHCID 81531DiisopropylethylamineHCID 151348Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 110737925-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic Acid

Product 1

HCID 54380946HCID 54380946, compoundYield 42%

Reagents, catalysts & solvents 3

HCID 962WaterSolventHCID 6228DimethylformamideSolventHCID 57417360Sodium chloride; waterSolvent

Procedure

To a mixture of 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (1.67 g, 10 mmol) in dimethylformamide (10 mL) was added benzotriazol-1-yloxytris(dimethylamino)-phosphonium hexafluorophosphate (BOP reagent, 6 g, 13.5 mmol) followed by 3 mL diisopropylethylamine. After stirring for 5 minutes, 1 mL of N,N-dimethylethylendiamine was added and the mixture was stirred at room temperature for 24 hours. To the reaction mixture was added 25 mL of 1N sodium hydroxide and 25 mL of brine. After stirring for 30 minutes, the reaction mixture was poured into water (100 mL) and extracted (3×200 mL) with 10% of methanol in dichloromethane. The organic layers were combined, dried over anhydrous sodium sulfate and evaporated using a rotary evaporator. The residue which remained was purified by chromatography (silica gel column, 5%-10% methanol in dichloromethane) to give 1 g (42%) of 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (2-dimethylamino-ethyl)-amide.

Workup

  1. stirringthe mixture was stirred at room temperature for 24 hours
  2. stirringAfter stirring for 30 minutes
  3. extractionextracted (3×200 mL) with 10% of methanol in dichloromethane
  4. dry with materialdried over anhydrous sodium sulfate
  5. customevaporated
  6. customa rotary evaporator
  7. customThe residue which remained was purified by chromatography (silica gel column, 5%-10% methanol in dichloromethane)

Sources & evidence

ORD record
ord-57b3be7798594c24848c742e499419ce
Source dataset
uspto-grants-2005_04
Patent number
US06878733B1

Reaction notes

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