Sodium Carbonate → 5-Hydroxy-2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-6-methyl-nicotinic acid methyl ester

HRID 329429Notes

Reaction equation

HRID 329429 reaction equation
[CH3:1][O:2][C:3](=[O:26])[C:4]1[CH:9]=[C:8]([O:10]C(=O)C)[C:7]([CH3:14])=[N:6][C:5]=1[C:15](=O)[NH:16][C:17]([C:22](=[O:24])[NH2:23])([CH3:21])[CH:18]([CH3:20])[CH3:19].P(Cl)(Cl)(Cl)(Cl)Cl.C(=O)([O-])[O-].[Na+].[Na+]>O=P(Cl)(Cl)Cl>[CH3:1][O:2][C:3](=[O:26])[C:4]1[CH:9]=[C:8]([OH:10])[C:7]([CH3:14])=[N:6][C:5]=1[C:15]1[NH:23][C:22](=[O:24])[C:17]([CH:18]([CH3:20])[CH3:19])([CH3:21])[N:16]=1

Participants

5

Procedure

A solution of 47 g (0.129 mol) 5-acetoxy-2-(1-carbamoyl-1,2-dimethylpropyl-carbamoyl)-6-methyl-nicotinic acid methyl ester and 93.8 g phosphorus pentachloride in 470 ml phosphoroxychloride is stirred 12 hours at room temperature. The solution is then hydrolysed with ice and neutralized with sodium carbonate. The product is extracted with ethyl acetate, the extract is then dried across magnesium sulfate and compressed. The crude product is recrystallized from ethyl acetate/isopropyl ester.

Workup

  1. extractionThe product is extracted with ethyl acetate
  2. dry with materialthe extract is then dried across magnesium sulfate
  3. customThe crude product is recrystallized from ethyl acetate/isopropyl ester

Sources & evidence

ORD record
ord-a39d1e917e664c3bb1f12678f59852d6
Source dataset
uspto-grants-1990_01
Patent number
US04891428

Reaction notes

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