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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775154Generated: October 31, 2026

Potassium Carbonate → (5-Bromo-6-fluoro-pyridin-2-yl)-(5-fluoro-6-methoxy-pyridin-3-ylmethyl)-amine

https://huagongshe.com/reaction/1775154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 57963067HCID 57963067—
SolventAcetonitrileHCID 6342—
Product(5-Bromo-6-fluoro-pyridin-2-yl)-(5-fluoro-6-methoxy-pyridin-3-ylmethyl)-amineHCID 5796322485.2%

Reaction Steps

To (5-fluoro-6-methoxy-pyridin-3-ylmethyl)-(6-fluoro-pyridin-2-yl)-amine (24, 3.21 g, 12.8 mmol) in 100 mL of acetonitrile, N-bromosuccinimide (2.30 g, 12.9 mmol) in 30 mL of acetonitrile was added slowly at room temperature. The reaction was stirred at room temperature for 4 hours, then poured into aqueous potassium carbonate and extracted with ethyl acetate. The organic layer was dried over sodium sulfate, filtered and the filtrate concentrated under vacuum. The resulting material was purified by silica gel column chromatography, eluting with 20% ethyl acetate in hexane. Appropriate fractions were combined and concentrated under vacuum to provide the desired compound (25, 3.60 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260437B2
Source datasetuspto-grants-2016_02
ORD IDord-0149bed51e424758b02656013360389e
Source noteuspto-grants-2016_02