Sodium Hydroxide → 1H-pyrrolo[2,3-b]pyridine-4-carboxylic acid

HRID 2182249Notes

Reaction equation

HRID 2182249 reaction equation
[NH:1]1[C:5]2[N:6]=[CH:7][CH:8]=[C:9]([C:10]([O:12]C)=[O:11])[C:4]=2[CH:3]=[CH:2]1.[OH-].[Na+]>CO>[NH:1]1[C:5]2[N:6]=[CH:7][CH:8]=[C:9]([C:10]([OH:12])=[O:11])[C:4]=2[CH:3]=[CH:2]1

Participants

4

Procedure

A solution of 1H-pyrrolo[2,3-b]pyridine-4 carboxylic acid, methyl ester [1.8 g, Reference Example 19(c)] in methanol (60 mL) was treated with sodium hydroxide solution (25 mL, 2N) and the mixture was stirred at room temperature for 2 hours then evaporated. The residue was treated with water (50 mL) and the pH of the mixture was adjusted to 34 by addition of hydrochloric acid. The resulting yellow solid was filtered, then washed well with water and then dried to give the title compound (1.1 g) as a yellow solid.

Workup

  1. customthen evaporated
  2. additionThe residue was treated with water (50 mL)
  3. additionthe pH of the mixture was adjusted to 34 by addition of hydrochloric acid
  4. filtrationThe resulting yellow solid was filtered
  5. washwashed well with water
  6. customdried

Sources & evidence

ORD record
ord-52585f93764c44a78bdddc8f1aeb8d47
Source dataset
uspto-grants-2005_05
Patent number
US06897207B2

Reaction notes

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