HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239398Generated: October 31, 2026
Tris(1,1-dimethylethyl)phosphine → HCID 25005983, compound
https://huagongshe.com/reaction/2239398
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | N-t-Butyl 4-bromobenzenesulfonamide | HCID 796629 | — |
| Reactant | (5-cyano-1-methyl-1H-pyrrol-2-yl)boronic acid | HCID 11708078 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | HCID 25005983 | HCID 25005983 | 15% |
Reaction Steps
According to general procedure B, 4-bromo-N-(tert-butyl)benzenesulfonamide (117 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. N-(tert-butyl)-4-(5-cyano-1-methyl-1H-pyrrol-2-yl)benzenesulfonamide (19 mg, 15%) was provided after purification. MS (ESI) m/z 317. HPLC purity 100.0% at 210-370 nm, 10.5 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 |
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| Patent number | US07723332B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-4d54e274e8be46c6a7fd898733ac8bbc |
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| Source note | uspto-grants-2010_05 |
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