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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium FluorideHCID 5235—
ReactantTrimethylsilyl 2,2-difluoro-2-(fluorosulfonyl)acetateHCID 2778022—
Reactant5-bromo-N-methyl-6-(N-methylmethylsulfonamido)-2-vinylbenzofuran-3-carboxamideHCID 90332428—
SolventTolueneHCID 1140—
SolventDiglymeHCID 8150—
Product5-bromo-2-(2,2-difluorocyclopropyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamideHCID 9033240422.9%

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242998B2
Source datasetuspto-grants-2016_01
ORD IDord-9a7a06fee25644c6aebd858da60e55fe
Source noteuspto-grants-2016_01