Triethylamine → 2-formyl-5-methyl-1H-pyrrole-3-carboxylic acid (2-diethylaminoethyl)-amide

HRID 1815352Notes

Reaction equation

HRID 1815352 reaction equation
[CH:1]([C:3]1[NH:4][C:5]([CH3:11])=[CH:6][C:7]=1[C:8]([OH:10])=O)=[O:2].C(N=C=NCCCN(C)C)C.C(N(CC)CC)C.[CH2:30]([N:32]([CH2:36][CH3:37])[CH2:33][CH2:34][NH2:35])[CH3:31]>CN(C)C=O.C(=O)(O)[O-].[Na+].[Cl-].[Na+].O>[CH2:30]([N:32]([CH2:36][CH3:37])[CH2:33][CH2:34][NH:35][C:8]([C:7]1[CH:6]=[C:5]([CH3:11])[NH:4][C:3]=1[CH:1]=[O:2])=[O:10])[CH3:31]

Participants

8

Procedure

To a solution of 2-formyl -5-methyl-1H-pyrrole-3-carboxylic acid (320 mg, 2.1 mmol) in dimethylformamide (3 mL) was added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (483 mg, 1.2 equivl.), 1-hydroxybenzotriaole (340 mg, 1.2 equiv.), triethylamine (0.59 mL, 2 equiv.) and N,N-diethylethylenediamine (0.32 mL, 1.1 equiv.). After stirring at room temperature overnight, the reaction was diluted with saturated sodium bicarbonate and brine (with extra salt) and extracted with 10% methanol in dichloromethane. The combined organic layers were washed with brine, dried over anhydrous sodium sulfate and concentrated to give 2-formyl-5-methyl-1H-pyrrole-3-carboxylic acid (2-diethylaminoethyl)-amide.

Workup

  1. extractionextracted with 10% methanol in dichloromethane
  2. washThe combined organic layers were washed with brine
  3. dry with materialdried over anhydrous sodium sulfate
  4. concentrationconcentrated

Sources & evidence

ORD record
ord-564f54cfcde44fc3870a2e258ec6e218
Source dataset
uspto-grants-2005_04
Patent number
US06878733B1

Reaction notes

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