HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473118Generated: November 1, 2026
Triethylamine → (R)-N-methyl-3-(2-(1-methylethylsulfonamido)-2,3-dihydro-1H-inden-5-yloxy)benzene sulfonamide
https://huagongshe.com/reaction/473118
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 3-boronobenzenesulfonamide | HCID 44886921 | — |
| Reactant | (R)-N-(5-hydroxy-2,3-dihydro-1H-inden-2-yl)propane-2-sulfonamide | HCID 68156499 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (R)-N-methyl-3-(2-(1-methylethylsulfonamido)-2,3-dihydro-1H-inden-5-yloxy)benzene sulfonamide | HCID 68155814 | — |
Reaction Steps
To a mixture of the 3-(N-methylsulfamoyl)phenylboronic acid (0.274 mmol, 59 mg), copper (II)acetate (0.137 mmol, 25 mg), triethylamine (0.685 mmol, 96 μL) and 4 Å molecular sieves (100 mg) in DCM (1 mL) was added (R)-N-(5-hydroxy-2,3-dihydro-1H-inden-2-yl)propane-2-sulfonamide (0.137 mmol, 35 mg) and the resultant mixture stirred at room temperature overnight. The reaction mixture was diluted with DCM (1 mL) before water (0.5 mL) was added and the organic layers separated using hydrophobic frits. The aqueous was extracted with further DCM (1 mL), and the combined organics concentrated using to dryness. The residue was taken up in DMSO and purified by preparative HPLC to give the title compound as a clear film (5.9 mg, 10.1%). MS (ESI): m/z [M−H]− 423.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633237B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-e2f61ae4af4c4e0f8b3bd5aec2e45fb5 |
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| Source note | uspto-grants-2014_01 |
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