Sodium Hydroxide → HCID 21254645, compound

HRID 2287602Notes

Reaction equation

HRID 2287602 reaction equation
C([O:3][C:4]([C:6]1[N:11]=[CH:10][C:9](/[CH:12]=[CH:13]/[C:14]([NH:16][CH2:17][C:18]([N:20]([C:22]2[C:23]([Cl:43])=[C:24]([C:39]([Cl:42])=[CH:40][CH:41]=2)[CH2:25][O:26][C:27]2[C:35]3[N:34]=[C:33]([O:36][CH3:37])[N:32]([CH3:38])[C:31]=3[CH:30]=[CH:29][CH:28]=2)[CH3:21])=[O:19])=[O:15])=[CH:8][CH:7]=1)=[O:5])C.[OH-].[Na+]>C(O)C>[C:4]([C:6]1[N:11]=[CH:10][C:9](/[CH:12]=[CH:13]/[C:14]([NH:16][CH2:17][C:18]([N:20]([C:22]2[C:23]([Cl:43])=[C:24]([C:39]([Cl:42])=[CH:40][CH:41]=2)[CH2:25][O:26][C:27]2[C:35]3[N:34]=[C:33]([O:36][CH3:37])[N:32]([CH3:38])[C:31]=3[CH:30]=[CH:29][CH:28]=2)[CH3:21])=[O:19])=[O:15])=[CH:8][CH:7]=1)([OH:5])=[O:3]

Participants

4

Procedure

To a solution of 4-[3-[N-[(E)-3-(6-ethoxycarbonylpyridin-3-yl)acryloylglycyl]-N-methylamino]-2,6-dichlorobenzyloxy]-2-methoxy-1-methyl-1H-benzimidazole (304 mg) in ethanol was added 1N sodium hydroxide solution (0.5 ml), and the mixture was stirred for 1.5 hours at ambient temperature. The solvent was removed, water was added to the residue. The mixture was adjusted to pH 4 with 1N hydrochloric acid and extracted with chloroform. The extract was dried and evaporated in vacuo. Acetonitrile was added to the residue, and the residue was collected by filtration to give 4-[3-[N-[(E)-3-(6-carboxypyridin-3-yl)acryloylglycyl]-N-methylamino]-2,6-dichlorobenzyloxy]-2-methoxy-1-methyl-1H-benzimidazole (195 mg).

Workup

  1. customThe solvent was removed
  2. additionwater was added to the residue
  3. extractionextracted with chloroform
  4. customThe extract was dried
  5. customevaporated in vacuo
  6. additionAcetonitrile was added to the residue
  7. filtrationthe residue was collected by filtration

Sources & evidence

ORD record
ord-d061cb9ac88945cbbcb6969d83eb9680
Source dataset
uspto-grants-2000_07
Patent number
US06083961

Reaction notes

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