HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239463Generated: October 30, 2026
Tris(1,1-dimethylethyl)phosphine → HCID 25005625, compound
https://huagongshe.com/reaction/2239463
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | (5-cyano-1-methyl-1H-pyrrol-2-yl)boronic acid | HCID 11708078 | — |
| Reactant | HCID 68482644 | HCID 68482644 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | HCID 25005625 | HCID 25005625 | 13% |
Reaction Steps
According to general procedure B, 4-bromo-2-fluoro-N-isopropylbenzenesulfonamide (177 mg, 0.59 mmol), 5-cyano-1-methyl-1H-pyrrol-2-ylboronic acid (106 mg, 0.70 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)-2-fluoro-N-isopropylbenzenesulfonamide (24 mg, 13%) was provided after purification. MS (ESI) m/z 321. HPLC purity 100.0% at 210-370 nm, 9.0 min.; the Xterrag 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-273a9b0533574015ba5887f58c19afc8 |
|---|
| Source note | uspto-grants-2010_05 |
|---|