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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595539Generated: October 29, 2026

Water → 5-bromo-2-iodo-N-methyl-6-(methylsulfonamido)benzofuran-3-carboxamide

https://huagongshe.com/reaction/595539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant6-amino-5-bromo-2-iodo-N-methylbenzofuran-3-carboxamideHCID 90332437—
SolventPyridineHCID 1049—
Product5-bromo-2-iodo-N-methyl-6-(methylsulfonamido)benzofuran-3-carboxamideHCID 9033239566.8%

Reaction Steps

To a solution of 6-amino-5-bromo-2-iodo-N-methylbenzofuran-3-carboxamide (1 g, 2.53 mmol) in pyridine, MsCl (580 mg, 5.06 mmol) was added dropwise at 0° C. The mixture was allowed to warm to room temperature and stirred for 1.5 h. After the solvent was removed, the reaction mixture was adjusted to pH=5-6 with 1 N HCl. After filtration, the solid was dissolved in THF:H2O=5:1 (15 mL) and then LiOH.H2O (800 mg, 20 mmol) was added. The mixture was stirred for 30 minutes at room temperature. After the solvent was removed, the reaction mixture was adjusted to pH=5-6 with 1 N HCl. Finally the precipitate was collected to give 5-bromo-2-iodo-N-methyl-6-(methylsulfonamido)benzofuran-3-carboxamide (800 mg, 90% purity by HPLC, yield: 60%), which was used for the next step without further purification. 1H-NMR (CDCl3, 400 MHz) δ 8.37 (s, 1H), 7.84 (s, 1H), 6.86 (s, 1H), 6.29 (s, 1H), 3.07 (d, J=4.8 Hz, 3H), 2.99 (s, 3H). MS (M+H)+: 473/475.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242998B2
Source datasetuspto-grants-2016_01
ORD IDord-782f6dfddd5b444eb7644cf671e071f0
Source noteuspto-grants-2016_01