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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279084Generated: October 30, 2026

HCID 86702340, compound → HCID 86702339, compound

https://huagongshe.com/reaction/2279084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86702340HCID 86702340—
SolventHydrogen BromideHCID 260—
ProductHCID 86702339HCID 86702339—

Reaction Conditions

Temperature100 °C

Reaction Steps

A suspension of 3-(5-chloro-2-methoxypyridin-3-yl)-N-[(1S)-1-(5-fluoropyridin-2-yl)ethyl]-3H-imidazo[4,5-b]pyridin-5-amine (Preparation 24d, 69 mg, 0.17 mmol) in aqueous hydrogen bromide solution (48%, 0.6 mL) was heated to 100° C. for 3 hours. After cooling to ambient temperature, water was removed under reduced pressure and the residue was treated with acetonitrile. The solid was filtered, washed with acetonitrile and dried to give the title compound as a hydrobromide salt (80 mg). The solid was then added to a stirred solution of aqueous saturated potassium carbonate (10 mL) and the resulting suspension was stirred for 2 hours. Ethyl acetate (15 mL) was added and the aqueous layer was separated and washed with ethyl acetate (2×15 mL). The combined organic extracts were dried over sodium sulphate and the solvents evaporated in vacuo to yield the title compound (44 mg, 66%) as a pink solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133200B2
Source datasetuspto-grants-2015_09
ORD IDord-3adf3bafb4d94a8f9e982e22f63b36b8
Source noteuspto-grants-2015_09