HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239492Generated: November 1, 2026
Tris(1,1-dimethylethyl)phosphine → HCID 25006737, compound
https://huagongshe.com/reaction/2239492
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 68481888 | HCID 68481888 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | HCID 25006737 | HCID 25006737 | 19% |
Reaction Steps
According to general procedure B, 4-bromo-N-tert-butyl-2-(trifluoromethoxy)benzenesulfonamide (225 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. N-tert-butyl-4-(5-cyano-1-methyl-1H-pyrrol-2-yl)-2-(trifluoromethoxy)benzenesulfonamide (44 mg, 19%) was provided after purification. MS (ESI) m/z 401. HPLC purity 99.0% at 210-370 nm, 10.1 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-94fb391e77654b939a34a98ae78f76ee |
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| Source note | uspto-grants-2010_05 |
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