Sodium Hydroxide → 5-Formyl-2-methyl-4-phenyl-1H-pyrrole-3-carboxylic acid (3-diethylamino-2-hydroxy-propyl)-amide

HRID 731161Notes

Reaction equation

HRID 731161 reaction equation
[CH:1]([C:3]1[NH:7][C:6]([CH3:8])=[C:5]([C:9]([OH:11])=O)[C:4]=1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=[O:2].[NH2:18][CH2:19][CH:20]([OH:27])[CH2:21][N:22]([CH2:25][CH3:26])[CH2:23][CH3:24].C1C=CC2N(O)N=NC=2C=1.C(=O)(O)[O-].[Na+].[OH-].[Na+]>C(Cl)(Cl)Cl>[CH2:23]([N:22]([CH2:25][CH3:26])[CH2:21][CH:20]([OH:27])[CH2:19][NH:18][C:9]([C:5]1[C:4]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[C:3]([CH:1]=[O:2])[NH:7][C:6]=1[CH3:8])=[O:11])[CH3:24]

Participants

7

Procedure

A mixture of 5-Formyl-2-methyl-4-phenyl-1H-pyrrole-3-carboxylic acid (1.0 gm, 4.36 mmol), 1-amino-3-diethylamino-2-propanol (950 mg, 6.54 mmol), DDC (900 mg, 4.36 mmol) and HOBt (884 mg, 6.54 mmol) in chloroform (60 mL) was stirred at rt for 12 hrs. The reaction was poured into sat. Sodium bicarbonate (60 mL) and to it was added 1N NaOH (8 mL). It was then extracted with EtOAc (3×100 mL), washed with water and brine, dried and concentrated to give 400 mg of 5-Formyl-2-methyl-4-phenyl-1H-pyrrole-3-carboxylic acid (3-diethylamino-2-hydroxy-propyl)-amide.

Workup

  1. extractionIt was then extracted with EtOAc (3×100 mL)
  2. washwashed with water and brine
  3. customdried
  4. concentrationconcentrated

Sources & evidence

ORD record
ord-85a71b16d5164905a63969f0e8698d41
Source dataset
uspto-grants-2009_09
Patent number
US07582756B2

Reaction notes

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