HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512025Generated: November 2, 2026
Potassium Carbonate → 4-({[5-Chloro-6-(3,3,3-trifluoropropoxy)pyridin-3-yl]oxy}methyl)-2,5-difluoro-N-(methylsulfonyl)benzamide
https://huagongshe.com/reaction/512025
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Chloro-6-(3,3,3-trifluoropropoxy)pyridin-3-ol | HCID 66666942 | — |
| Reactant | 4-(Bromomethyl)-2,5-difluoro-N-(methylsulfonyl)benzamide | HCID 66667111 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-({[5-Chloro-6-(3,3,3-trifluoropropoxy)pyridin-3-yl]oxy}methyl)-2,5-difluoro-N-(methylsulfonyl)benzamide | HCID 86682566 | 78.6% |
Reaction Steps
Potassium carbonate (61 mg, 0.229 mmol) was added to a solution of 5-chloro-6-(3,3,3-trifluoropropoxy)pyridin-3-ol (Preparation 67, 45 mg, 0.19 mmol) in DMSO (2 mL) and the reaction mixture was stirred under a nitrogen atmosphere at room temperature for 5 minutes. 4-(Bromomethyl)-2,5-difluoro-N-(methylsulfonyl)benzamide (Preparation 10, 63 mg, 0.19 mmol) was then added and the resulting mixture stirred under nitrogen at room temperature for 120 hours. The reaction mixture was diluted with aqueous hydrochloric acid solution (2 M, 15 mL), extracted with EtOAc (20 mL). The organic layer was washed with aqueous hydrochloric acid solution (2 M, 2×10 mL), dried over magnesium sulfate, filtered and evaporated in vacuo. The resulting crude solid was triturated with TBME/heptane (2:1), washed with heptane and dried in vacuo to yield the title compound as an off-white solid (73 mg, 74%):
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09102621B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-3977a7a4b105426f955c028fdad0c22e |
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| Source note | uspto-grants-2015_08 |
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