Water → HCID 66958389, compound

HRID 2283917Notes

Reaction equation

HRID 2283917 reaction equation
[O:1]=[C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4](=[O:11])[N:3]1[CH2:12][C:13]1[N:17]([CH3:18])[N:16]=[C:15]([C:19]([O:21]CC)=[O:20])[CH:14]=1.O>Cl.C(O)(=O)C>[O:11]=[C:4]1[C:5]2[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=2)[C:2](=[O:1])[N:3]1[CH2:12][C:13]1[N:17]([CH3:18])[N:16]=[C:15]([C:19]([OH:21])=[O:20])[CH:14]=1

Participants

5

Procedure

A solution of ethyl 5-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-1-methyl-1H-pyrazole-3-carboxylate (8.13 g, 25.9 mmol) in hydrochloric acid (33 mL of 1 M) and acetic acid (33 mL) was heated at reflux intermittently for six hours and allowed to cool to room temperature; a precipitate formed. Water was added, and the solid was isolated by filtration, washed with water, and dried on the vacuum filter funnel for two days to provide 3.79 g of 5-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-1-methyl-1H-pyrazole-3-carboxylic acid as a brown solid.

Workup

  1. temperatureat reflux intermittently for six hours
  2. customa precipitate formed
  3. customthe solid was isolated by filtration
  4. washwashed with water
  5. customdried on the vacuum
  6. filtrationfilter funnel for two days

Sources & evidence

ORD record
ord-c0fe863c2b1b43dea3d508732ce91c29
Source dataset
uspto-grants-2015_09
Patent number
US09145410B2

Reaction notes

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