HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590782Generated: October 29, 2026
Selenium Dioxide → 6-chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridine-4-carbaldehyde
https://huagongshe.com/reaction/590782
Participants
| Role | Name | HCID | Charge |
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| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | 6-chloro-3-iodo-4-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridine | HCID 118168962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridine-4-carbaldehyde | HCID 118168950 | 53.1% |
Reaction Steps
6-Chloro-3-iodo-4-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridine (20 g, 37.3 mmol) was dissolved in dioxane (400 mL) and selenium dioxide (12.43 g, 112 mmol) was added. The reaction mixture was stirred at 100° C. for 6 hrs. Selenium dioxide (4.14 g, 37.3 mmol) was added and the reaction mixture continued stirring at 100° C. overnight. The reaction was filtered over celite, rinsed with DCM, and concentrated in vacuo. The residue was dissolved in DCM (1.0 L) and filtered over celite. The material was concentrated in vacuo while loading on silica gel. Purification by flash chromatography (0-5% DCM/EtOAc) gave 6-chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridine-4-carbaldehyde (10.88 g, 19.79 mmol, 53.0%). 1H NMR (ppm, 500 MHz, DMSO-d6) δ 10.54 (s, 1H), 7.39-7.35 (m, 10H), 7.17-7.11 (m, 5H), 6.29 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09233979B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-299e10dbf97d4f3787a2f469f8d5c7c2 |
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| Source note | uspto-grants-2016_01 |
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