HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186790Generated: November 1, 2026
Dichloromethane → 1-(3-Sulfamoylphenyl)-1H-pyrazolo[3,4-b]pyridin-4-ylboronic acid
https://huagongshe.com/reaction/1186790
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Bis(pinacolato)diborane | HCID 2733548 | — |
| Reactant | 3-(4-iodo-1H-pyrazolo[3,4-b]pyridin-1-yl)benzenesulfonamide | HCID 66664861 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-(3-Sulfamoylphenyl)-1H-pyrazolo[3,4-b]pyridin-4-ylboronic acid | HCID 66668003 | — |
Reaction Steps
To a 48 mL pressure bottle was added 3-(4-iodo-1H-pyrazolo[3,4-b]pyridin-1-yl)benzenesulfonamide, “dot” 2 1-methyl-2-pyrrolidinone complex (60 mg, 0.100 mmol), 4,4,4′,4′,5,5,5′,5′-octamethyl-2,2′-bi(1,3,2-dioxaborolane) (94.7 mg, 0.373 mmol), potassium acetate (24.4 mg, 0.249 mmol) and anhydrous DMSO (Volume: 2 mL). The reaction mixture was purged well with argon and treated with PdCl2(dppf).CH2Cl2 (12.5 mg, 0.017 mmol). The reaction mixture was then heated to 84° C. for 1 h to give the desired intermediate. LC/MS (Condition B): ret. T=2.4 min, (M+H)+ 318.98.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08673922B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-1e76399b7ba24a718af6a74a4c700551 |
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| Source note | uspto-grants-2014_03 |
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