HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595586Generated: October 30, 2026
Sodium Fluoride → 5-bromo-2-(2,2-difluorocyclopropyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide
https://huagongshe.com/reaction/595586
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Fluoride | HCID 5235 | — |
| Reactant | Trimethylsilyl 2,2-difluoro-2-(fluorosulfonyl)acetate | HCID 2778022 | — |
| Reactant | 5-bromo-N-methyl-6-(N-methylmethylsulfonamido)-2-vinylbenzofuran-3-carboxamide | HCID 90332428 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | 5-bromo-2-(2,2-difluorocyclopropyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide | HCID 90332404 | 22.9% |
Reaction Steps
A solution of trimethylsilyl 2-fluorosulfonyl-2,2-difluoroacetate (31 mg, 0.12 mmol) in toluene (0.5 mL) was added dropwise to a solution of 5-bromo-N-methyl-6-(N-methylmethylsulfonamido)-2-vinylbenzofuran-3-carboxamide (30 mg, 0.07 mmol) and NaF (1 mg, 0.02 mmol) in diglyme (1 mL) at 120° C. over 15 min. The mixture was then stirred at 120° C. for 2 h. The mixture was concentrated in vacuum and the residue was purified by prep-TLC (PE:EA=1:1) to give the product of 5-bromo-2-(2,2-difluorocyclopropyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide (7 mg, yield: 22%). 1H-NMR (DMSO-d6, 400 MHz) δ 8.13 (s, 1H), 8.02 (s, 1H), 3.74˜3.66 (m, 1H), 3.19 (s, 3H), 3.18 (s, 3H), 2.84 (s, 3H), 2.38˜2.39 (m, 1H), 2.21˜2.17 (m, 1H). MS (M+H)+: 437/439.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242998B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-9a7a06fee25644c6aebd858da60e55fe |
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| Source note | uspto-grants-2016_01 |
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