Sodium Hydroxide → HCID 11530248, compound

HRID 1445618Notes

Reaction equation

HRID 1445618 reaction equation
C[O:2][C:3](=[O:25])[CH2:4][C:5]1[C:13]2[C:8](=[N:9][CH:10]=[CH:11][CH:12]=2)[N:7]([CH2:14][C:15]2[CH:20]=[CH:19][C:18]([S:21]([CH3:23])=[O:22])=[CH:17][CH:16]=2)[C:6]=1[CH3:24].[OH-].[Na+]>C1COCC1.CO>[CH3:23][S:21]([C:18]1[CH:19]=[CH:20][C:15]([CH2:14][N:7]2[C:8]3=[N:9][CH:10]=[CH:11][CH:12]=[C:13]3[C:5]([CH2:4][C:3]([OH:25])=[O:2])=[C:6]2[CH3:24])=[CH:16][CH:17]=1)=[O:22]

Participants

4

Procedure

To a stirred solution of [1-(4-methanesulfinyl-benzyl)-2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl]-acetic acid methyl ester (0.340 g, 0.95 mmol) in THF/MeOH (8 ml of a 1:1 mixture) is added 1M NaOH (2 ml) and the reaction mixture is stirred for 2 hours. The solvent is removed in vacuo and the resulting oil is dissolved in water and acidified to pH2 using concentrated HCl. A precipitate forms which is filtered, washed with water and dried in vacuo to yield the titled product. (MH+ 343)

Workup

  1. customThe solvent is removed in vacuo
  2. dissolutionthe resulting oil is dissolved in water
  3. filtrationA precipitate forms which is filtered
  4. washwashed with water
  5. customdried in vacuo

Sources & evidence

ORD record
ord-3dfd846560fd45a093f9373cd6d70d47
Source dataset
uspto-grants-2010_02
Patent number
US07666878B2

Reaction notes

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