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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888397Generated: October 29, 2026

Potassium Fluoride → 6-Bromo-9H-pyrrolo[2,3-b:5,4-c′]dipyridine

https://huagongshe.com/reaction/1888397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 58266636HCID 58266636—
SolventTetrahydrofuranHCID 8028—
Product6-Bromo-9H-pyrrolo[2,3-b:5,4-c′]dipyridineHCID 5826672775%

Reaction Steps

A solution of 6′-bromo-2-fluoro-[3,4′]bipyridinyl-3′-ylamine (7.22 g, 26.9 mmol) in THF (75 mL) was added dropwise over 10 minutes to sodium bis-(trimethylsilyl)amide (1N solution in THF, 54 mL, 53.9 mmol). The reaction mixture was left to stir for 2.5 h then 1N aqueous potassium fluoride solution (7 mL) was added and the solvent evaporated in vacuo. The residue was diluted with water (100 mL) and the resultant solid was collected by filtration, washed with water (20 mL) and diethyl ether:pentane (1:1, 20 mL) and left to air dry. The resultant solid was triturated with methanol (50 mL), collected by filtration, washed with methanol (10 mL) and diethyl ether (20 mL) and pentane (20 mL) and left to air dry to afford the title compound as a brown solid (5.0 g, 75%). 1H NMR (DMSO-D6, 300 MHz): 8.73-8.69 (m, 2H), 8.63 (dd, J=4.8, 1.7 Hz, 1H), 8.48 (dd, J=1.0 Hz, 1H), 7.33 (dd, J=7.8, 4.8 Hz, 1H). LCMS (Method B): RT=2.43 min, M+H+=248/250.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501765B2
Source datasetuspto-grants-2013_08
ORD IDord-1ae3d4eb9fbf46e5b9c2108af4291a4b
Source noteuspto-grants-2013_08