Sodium Hydroxide → 4-Chloro-1H-pyrrolo[2,3-b]pyridine
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]=12Participants
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
- temperatureThe mixture was cooled to room temperature
- distillationmost of the POCl3 was distilled off under high vacuum
- dissolutionThe residue was dissolved in CH3CN (10 mL)
- additionWater (20 mL) was added slowly
- customto quench
- customthe reaction
- filtrationThe solid was filtered
- 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
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