HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239501Generated: October 30, 2026
Tris(1,1-dimethylethyl)phosphine → HCID 25006742, compound
https://huagongshe.com/reaction/2239501
Participants
| Role | Name | HCID | Charge |
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| 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 | Benzenesulfonamide, 4-bromo-N-(cyclopropylmethyl)-2,5-difluoro- | HCID 68482433 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | HCID 25006742 | HCID 25006742 | 26.8% |
Reaction Steps
According to general procedure B, 4-bromo-N-(cyclopropylmethyl)-2,5-difluorobenzenesulfonamide (150 mg, 0.5 mmol), 5-cyano-1-methyl-1H-pyrrol-2-ylboronic acid (90 mg, 0.60 mmol), potassium fluoride (96 mg, 1.65 mmol), and tris(dibenzylideneacetone)dipalladium (12 mg, 0.013 mmol) were placed in an oven dried flask under nitrogen and dry THF (1.3 mL) was added. Tri-t-butylphosphine (75 μL, 0.026 mmol, 10 wt % in hexane) was added and the reaction was stirred for 16 hours. Purification afforded 4-(5-cyano-1-methyl-1H-pyrrol-2-yl)-N-(cyclopropylmethyl)-2,5-difluorobenzenesulfonamide (47 mg). HPLC purity 98.2% at 210-370 nm, 9.5 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. HRMS: calcd for C16H15F2N3O2S−H+, 350.07803; found (ESI-FTMS, [M−H]1−), 350.07826
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-2048167462d54e08974f0ad71cc99d58 |
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| Source note | uspto-grants-2010_05 |
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