Hydrochloric Acid → HCID 178439578, compound

HRID 980557Notes

Reaction equation

HRID 980557 reaction equation
[C:1]([C:4]([NH:9][C:10]([C:12]1[C:21]([C:22]([OH:24])=[O:23])=[CH:20][C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[N:13]=1)=O)([CH3:8])[CH:5]([CH3:7])[CH3:6])(=[O:3])[NH2:2].[OH-].[Na+].Cl>O>[CH:5]([C:4]1([CH3:8])[NH:9][C:10]([C:12]2[C:21]([C:22]([OH:24])=[O:23])=[CH:20][C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[N:13]=2)=[N:2][C:1]1=[O:3])([CH3:7])[CH3:6]

Participants

5

Procedure

A solution of 2-[(1-carbamoyl-1,2-dimethylpropyl)carbamoyl]-3-quinolinecarboxylic acid (0.152 mol), in water (50 ml) containing sodium hydroxide (0.06 mol) is heated at 75° to 80° C. for 2 hours. The solution is cooled in an ice bath and acidified with concentrated hydrochloric acid, added in small increments. The resulting precipitate is filtered, washed with water, air dried, and recrystallized from acetone to afford the 2-(5-isopropyl-5-methyl-4-oxo-2-imidazolin-2-yl)-3-quinolinecarboxylic acid, mp 239°-243.5° C.

Workup

  1. temperatureis heated at 75° to 80° C. for 2 hours
  2. temperatureThe solution is cooled in an ice bath
  3. additionadded in small increments
  4. filtrationThe resulting precipitate is filtered
  5. washwashed with water, air
  6. customdried
  7. customrecrystallized from acetone

Sources & evidence

ORD record
ord-29dbd4883ee74f578e820f562c1f2fc7
Source dataset
uspto-grants-1987_01
Patent number
US04638068

Reaction notes

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