Hydrochloric Acid → HCID 22504429, compound

HRID 1432243Notes

Reaction equation

HRID 1432243 reaction equation
[F:1][C:2]1[CH:31]=[CH:30][C:5]([CH2:6][N:7]2[C:15]3[C:10](=[CH:11][C:12]([S:16]([CH3:19])(=[O:18])=[O:17])=[CH:13][CH:14]=3)[CH:9]=[C:8]2[C:20]2[CH:25]=[CH:24][C:23]([C:26]([O:28]C)=[O:27])=[CH:22][N:21]=2)=[CH:4][CH:3]=1.[OH-].[K+].CO.Cl>O>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][N:7]2[C:15]3[C:10](=[CH:11][C:12]([S:16]([CH3:19])(=[O:17])=[O:18])=[CH:13][CH:14]=3)[CH:9]=[C:8]2[C:20]2[CH:25]=[CH:24][C:23]([C:26]([OH:28])=[O:27])=[CH:22][N:21]=2)=[CH:30][CH:31]=1

Participants

6

Procedure

A mixture of 1-(4-fluorobenzyl)-5-methanesulfonyl-2-(5-methoxycarbonylpyridin-2-yl)indole (0.37 g), potassium hydroxide (0.12 g) and methanol (40 ml) was heated under reflux for 3 hours under nitrogen atmosphere. To the reaction solution was added water and the mixture was neutralized with hydrochloric acid. The precipitated crystal was filtered off. The resulting crude crystal was recrystallized (ethanol) to obtain 0.35 g of the desired product.

Workup

  1. temperaturewas heated
  2. temperatureunder reflux for 3 hours under nitrogen atmosphere
  3. filtrationThe precipitated crystal was filtered off
  4. customThe resulting crude crystal was recrystallized (ethanol)

Sources & evidence

ORD record
ord-9c752545065d41d18684272e7b36fb5a
Source dataset
uspto-grants-2009_11
Patent number
US07612070B2

Reaction notes

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