HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183583Generated: October 30, 2026
Phosphorus oxychloride → HCID 136011334, compound
https://huagongshe.com/reaction/2183583
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 135713177 | HCID 135713177 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 136011334 | HCID 136011334 | 73% |
Reaction Steps
A solution of ethyl 4-hydroxy-1-methyl-6-oxo-6,7-dihyrdo-1H-pyrazolo-[3,4-b]pyridine-5-carboxylate (10 g, 42.2 mmol) in acetonitrile is treated with benzyl triethyl ammonium chloride (40.4 g, 169 mmol), followed by phosphorous oxychloride (17.6 mL, 190 mmol), heated at 40° C. for 0.5 h, then at reflux temperature for 2.5 h, cooled to room temperature, diluted with water (caution exotherm), stirred at ambient temperatures for 16 h and filtered. The filtercake is washed with cyclohexane and dried in vacuo to give the title compound as a white solid, 7.87 g (73% yield), identified by HNMR analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06900223B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-297aa9f68649467799a850d9ee36dd2a |
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| Source note | uspto-grants-2005_05 |
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