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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | 6-amino-5-bromo-2-iodo-N-methylbenzofuran-3-carboxamide | HCID 90332437 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 5-bromo-2-iodo-N-methyl-6-(methylsulfonamido)benzofuran-3-carboxamide | HCID 90332395 | 66.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09242998B2 |
|---|
| Source dataset | uspto-grants-2016_01 |
|---|
| ORD ID | ord-782f6dfddd5b444eb7644cf671e071f0 |
|---|
| Source note | uspto-grants-2016_01 |
|---|