HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892563Generated: October 31, 2026
Water → 4-fluoro-5-(3-fluoro-2-methyl-5-(3-(pyrimidin-2-yl)oxetan-3-ylcarbamoyl)phenyl)-2-(4-fluorophenyl)-N-methylbenzofuran-3-carboxamide
https://huagongshe.com/reaction/1892563
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | 3-Fluoro-5-(4-fluoro-2-(4-fluorophenyl)-3-(methylcarbamoyl)benzofuran-5-yl)-4-methylbenzoic acid | HCID 58472900 | — |
| Reactant | 3-(Pyrimidin-2-yl)oxetan-3-amine hydrochloride | HCID 67957812 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-fluoro-5-(3-fluoro-2-methyl-5-(3-(pyrimidin-2-yl)oxetan-3-ylcarbamoyl)phenyl)-2-(4-fluorophenyl)-N-methylbenzofuran-3-carboxamide | HCID 67957715 | — |
Reaction Steps
To a yellow solution mixture of 3-fluoro-5-(4-fluoro-2-(4-fluorophenyl)-3-(methylcarbamoyl)benzofuran-5-yl)-4-methylbenzoic acid (30 mg, 0.068 mmol) and 3-(pyrimidin-2-yl)oxetan-3-amine hydrochloride (12.5 mg, 0.067 mmol) in DMF (1 ml) in a 25 mL round-bottomed flask was added PyBOP (50 mg, 0.096 mmol), followed by TEA (0.1 ml, 0.717 mmol), and the reaction mixture was stirred for overnight. Ice cooled water was added to the reaction mixture, which was then stirred for 10-15 min. at 0° C. Precipitation was observed. The solid was collected by filtration, washed with cold water, and then dissolved in dichloromethane. The organic was dried over Na2SO4, filtered and concentrated. The crude product was purified by preparative HPLC. Yield (10 mg, 25%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507683B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-6e1d7347c85e4bb485a5d90cf2f6bcc0 |
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| Source note | uspto-grants-2013_08 |
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