HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239481Generated: October 30, 2026
Potassium Fluoride → HCID 25006359, compound
https://huagongshe.com/reaction/2239481
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | (5-cyano-1-methyl-1H-pyrrol-2-yl)boronic acid | HCID 11708078 | — |
| Reactant | HCID 68481891 | HCID 68481891 | — |
| Catalyst | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | HCID 25006359 | HCID 25006359 | 35% |
Reaction Steps
According to general procedure B, 4-bromo-N-isopropyl-2-(trifluoromethoxy)benzenesulfonamide (217 mg, 0.59 mmol), 5-cyano-1-methyl-1H-pyrrol-2-ylboronic acid (107 mg, 0.71 mmol), potassium fluoride (113 mg, 1.95 mmol), and tris(dibenzylideneacetone)dipalladium (0) (15 mg, 0.01 mmol) were placed in an oven dried flask under nitrogen and dry THF (1.4 mL) was added. Tri-t-butylphosphine (89 μL, 0.02 mmol, 10 wt % in hexane) was added and the reaction was stirred for 16 hours. 4-(5-cyano-1-methyl-1H-pyrrol-2-yl)-N-isopropyl-2-(trifluoromethoxy)benzenesulfonamide (79 mg, 35%) was provided after purification. MS (ESI) m/z 387. HPLC purity 100.0% at 210-370 nm, 9.8 min.; the Xterra® RP18 column, 3.5μ, 150×4.6 mm column, 1.2 mL/min., 85/15-5/95 (ammonium formate buffer pH=3.5/ACN+MeOH) for 10 min., hold 4 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07723332B2 |
|---|
| Source dataset | uspto-grants-2010_05 |
|---|
| ORD ID | ord-7025cf9a540d49648686a5ccc969a743 |
|---|
| Source note | uspto-grants-2010_05 |
|---|