HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279084Generated: October 30, 2026
HCID 86702340, compound → HCID 86702339, compound
https://huagongshe.com/reaction/2279084
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86702340 | HCID 86702340 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Product | HCID 86702339 | HCID 86702339 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133200B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-3adf3bafb4d94a8f9e982e22f63b36b8 |
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| Source note | uspto-grants-2015_09 |
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