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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506021Generated: October 29, 2026

Sodium bis(trimethylsilyl)amide → 3-Bromo-6-fluoro-9H-dipyrido[2,3-b;4',3'-d]pyrrole

https://huagongshe.com/reaction/1506021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant5-Bromo-2,6'-difluoro-[3,4]bipyridinyl-3'-ylamineHCID 58266654—
SolventTetrahydrofuranHCID 8028—
Product3-Bromo-6-fluoro-9H-dipyrido[2,3-b;4',3'-d]pyrroleHCID 58266831—

Reaction Steps

A solution of 5-bromo-2,6′-difluoro-[3,4′]bipyridinyl-3′-ylamine (0.79 g, 2.76 mmol) in THF (15 mL) was added dropwise over 10 minutes to sodium bis(trimethylsilyl)amide (1N solution in THF, 5.5 mL, 5.52 mmol). The reaction mixture was left to stir for 20 minutes then quenched by the addition of water (2 mL). The resultant black solution was partitioned between ethyl acetate (75 mL) and water (50 mL) and the layers separated. The organic phase was dried over sodium sulfate, filtered and evaporated in vacuo to give an off white solid. The resultant solid was triturated with ethyl acetate (30 mL), collected by filtration, washed with diethyl ether (5 mL) and left to air dry to afford the title compound as an off white solid (0.51 g, 65%). 1H NMR (DMSO-D6, 300 MHz): 9.00 (d, J=2.3 Hz, 1H), 8.69 (d, J=2.3 Hz, 1H), 8.51 (dd, J=1.7, 0.9 Hz, 1H), 7.95 (dd, J=2.4, 0.9 Hz, 1H). LCMS (Method B): RT=3.10 min, M+H+=266/268.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216980B2
Source datasetuspto-grants-2015_12
ORD IDord-039fb25c5e0e40c1ba8c12571f9e6fb0
Source noteuspto-grants-2015_12