Hydrochloric Acid → HCID 68511825, compound

HRID 2240205Notes

Reaction equation

HRID 2240205 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[C:9](=[O:13])[N:8]([CH2:14][CH2:15][CH2:16][N:17]1C(=O)C3C(=CC=CC=3)C1=O)[C:7]([CH3:28])=[C:6]2[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1.NN.[ClH:37]>CO.[Cl-].[Na+].O>[Cl-:37].[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[C:9](=[O:13])[N:8]([CH2:14][CH2:15][CH2:16][NH3+:17])[C:7]([CH3:28])=[C:6]2[C:29]1[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=1

Participants

6

Procedure

2-[3-(6-methoxy-3-methyl-1-oxo-4-phenylisoquinolin-2(1H)-yl)propyl]-1H-isoindole-1,3(2H)-dione (0.46 g) was dissolved in 20 mL methanol, and hydrazine (0.100 mL) was added. The reaction was stirred overnight at room temp, then diluted with brine and extracted with EtOAc (3×). The combined organic solutions were dried (Na2SO4) and concentrated. Flash chromatography (5% MeOH in CH2Cl2) gave a solid, which was treated with excess HCl and recrystallized from isopropanol/diethyl ether to give the titled compound.

Workup

  1. extractionextracted with EtOAc (3×)
  2. dry with materialThe combined organic solutions were dried (Na2SO4)
  3. concentrationconcentrated
  4. customFlash chromatography (5% MeOH in CH2Cl2) gave a solid, which
  5. customrecrystallized from isopropanol/diethyl ether

Sources & evidence

ORD record
ord-54d0702e08e74e48a61cdb0c3babb39c
Source dataset
uspto-grants-2010_05
Patent number
US07723352B2

Reaction notes

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