HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048025Generated: November 2, 2026
Potassium Carbonate → 5-Chloro-4-(5-chloro-6-(3,3-difluoroazetidin-1-yl)pyridin-3-yloxy)-2-fluoro-N-(methylsulfonyl)benzamide
https://huagongshe.com/reaction/2048025
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,3-Difluoroazetidine hydrochloride | HCID 2758247 | — |
| Reactant | 5-Chloro-4-[(5-chloro-6-fluoropyridin-3-yl)oxy]-2-fluoro-N-(methylsulfonyl)benzamide | HCID 58042437 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Chloro-4-(5-chloro-6-(3,3-difluoroazetidin-1-yl)pyridin-3-yloxy)-2-fluoro-N-(methylsulfonyl)benzamide | HCID 58042359 | 25% |
Reaction Steps
3,3-Difluoroazetidine hydrochloride (98 mg, 0.76 mmol) was added to a suspension of 5-chloro-4-(5-chloro-6-fluoropyridin-3-yloxy)-2-fluoro-N-(methylsulfonyl)benzamide (Example 19, 150 mg, 0.38 mmol) and potassium carbonate (74 mg, 0.53 mmol) in dimethylsulfoxide (1 mL). The reaction mixture was stirred at 90° C. in the microwave for 15 hours. The reaction mixture was diluted with water (10 mL) and extracted with ethyl acetate (3×10 mL). The combined organic layers were dried (MgSO4), filtered and concentrated in vacuo. The crude compound was purified by reverse phase preparative HPLC eluting with acetonitrile:water (from 5:95 to 95:5) to give the title compound as a colourless solid (44 mg, 25%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592629B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-153c05bd946446469fa10c2e50398876 |
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| Source note | uspto-grants-2013_11 |
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