HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239414Generated: November 3, 2026
Tris(1,1-dimethylethyl)phosphine → HCID 25004588, compound
https://huagongshe.com/reaction/2239414
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | HCID 3845777 | HCID 3845777 | — |
| Reactant | (5-cyano-1-methyl-1H-pyrrol-2-yl)boronic acid | HCID 11708078 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | HCID 25004588 | HCID 25004588 | 5% |
Reaction Steps
According to general procedure B, 4-bromo-N-(cyclopropylmethyl)benzenesulfonamide (116 mg, 0.40 mmol), 5-cyano-1-methyl-1H-pyrrol-2-ylboronic acid (72 mg, 0.48 mmol), potassium fluoride (76 mg, 1.3 mmol), and tris(dibenzylideneacetone)dipalladium(0) (10 mg, 0.01 mmol) were placed in an oven dried flask under nitrogen and dry THF (1.0 mL) was added. Tri-t-butylphosphine (60 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-(cyclopropylmethyl)benzenesulfonamide (6 mg, 5%) was provided after purification. MS (ESI) m/z 315. HPLC purity 100.0% at 210-370 mn, 10.3 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-67812fbe48d4470b83ee99fbbd700a2e |
|---|
| Source note | uspto-grants-2010_05 |
|---|