HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802889Generated: October 26, 2026
N,N'-Dimethylethylenediamine → 4-(cyclopropylsulfonyl)-1H-pyrazolo[3,4-b]pyridine
https://huagongshe.com/reaction/1802889
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium cyclopropanesulfinate | HCID 42643363 | — |
| Reactant | 4-Iodo-1H-pyrazolo[3,4-b]pyridine | HCID 57642801 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-(cyclopropylsulfonyl)-1H-pyrazolo[3,4-b]pyridine | HCID 57964109 | 9% |
Reaction Steps
To a solution of 4-iodo-1H-pyrazolo[3,4-b]pyridine (5.2 g) in dimethyl sulfoxide (70 mL) were added N,N′-dimethylethylenediamine (114 μL), copper (I) iodide (202 mg), sodium cyclopropanesulfinate (8.16 g) and potassium carbonate (5.06 g) at room temperature under argon atmosphere, and the mixture was stirred at 100° C. for 16 hr. The reaction mixture was filtered, water was added to the filtrate, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4), and concentrated. The obtained residue was subjected to silica gel column chromatography to give the title compound (0.42 g, yield 9%) as yellow crystals from the fraction eluted with ethyl acetate-hexane (1:1, volume ratio). MS: 224 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08349886B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-0a58d9542a994a4c8bc0e0482c449355 |
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| Source note | uspto-grants-2013_01 |
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