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

HRID 1910733Notes

Reaction equation

HRID 1910733 reaction equation
[NH:1]1[C:5]2=[N+:6]([O-])[CH:7]=[CH:8][CH:9]=[C:4]2[CH:3]=[CH:2]1.O=P(Cl)(Cl)[Cl:13].[OH-].[Na+]>>[Cl:13][C:9]1[CH:8]=[CH:7][N:6]=[C:5]2[NH:1][CH:2]=[CH:3][C:4]=12

Participants

4

Conditions

Temperature
106 °C

Procedure

The m-CBA salt of 1H-Pyrrolo[2,3-b]pyridine 7-oxide (9 g) was taken into POCl3 (46 mL, 7.5 eq.). The mixture was heated at 90° C. for 15 hours and to 106° C. for another 4 hours. The mixture was cooled to room temperature, and most of the POCl3 was distilled off under high vacuum. The residue was dissolved in CH3CN (10 mL). Water (20 mL) was added slowly to quench the reaction. The resulted mixture was adjusted to pH 9 using 10 N NaOH. The solid was filtered. The crude solid was redissolved in several ml of THF and combiflashed using 0-10% MeOH in DCM to give 4-Chloro-1H-pyrrolo[2,3-b]pyridine as a slightly yellowish solid. (4 g). MS: m/z 154.9 [MH+].

Workup

  1. temperatureThe mixture was cooled to room temperature
  2. distillationmost of the POCl3 was distilled off under high vacuum
  3. dissolutionThe residue was dissolved in CH3CN (10 mL)
  4. additionWater (20 mL) was added slowly
  5. customto quench
  6. customthe reaction
  7. filtrationThe solid was filtered
  8. dissolutionThe crude solid was redissolved in several ml of THF

Sources & evidence

ORD record
ord-a7850671af2a4803b6bb3cd1f3eac047
Source dataset
uspto-grants-2013_12
Patent number
US08604031B2

Reaction notes

Loading…