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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019588Generated: November 1, 2026

Potassium Hydroxide → 5-Fluoro-1-(3-fluorobenzyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid

https://huagongshe.com/reaction/1019588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant5-fluoro-1-(3-fluorobenzyl)-1H-pyrrolo[2,3-b]pyridine 2-ethyl carboxylateHCID 86639062—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product5-Fluoro-1-(3-fluorobenzyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acidHCID 6690794390.2%

Reaction Steps

A mixture of 6.9 g (20.58 mmol) of 5-fluoro-1-(3-fluorobenzyl)-1H-pyrrolo[2,3-b]pyridine-2-ethyl carboxylate (WO07/010,138) and 1.89 g (33.7 mmol) of potassium hydroxide in a mixture of 80 mL of ethanol and 10 mL of water is heated under reflux for 1.5 h. After this time, the reaction mixture is concentrated at reduced pressure, and is then taken up in 200 mL of water. The solution is acidified with additions of concentrated hydrochloric acid, and then extracted three times with 50 mL of dichloromethane. The organic phases are combined, dried over sodium sulfate and then concentrated at reduced pressure. The resultant product is triturated in 5 mL of dichloromethane. A precipitate is collected by filtration and is dried at reduced pressure. In this way we isolate 5.35 g of the expected product, which is used as it is in the rest of the synthesis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716273B2
Source datasetuspto-grants-2014_05
ORD IDord-32e3f5a990c44f2ca519cdc595ddddd1
Source noteuspto-grants-2014_05