HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175393Generated: October 29, 2026
p-Toluenesulfonic acid → HCID 86721325, compound
https://huagongshe.com/reaction/2175393
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178510199 | HCID 178510199 | — |
| Product | HCID 86721325 | HCID 86721325 | 80% |
Reaction Steps
5-(5-chloro-4-hydroxypyrimidin-2-ylamino)-2-cyclopropylbenzonitrile, containing 1.2 equivalents of p-toluenesulfonic acid (1.00 g, 2.03 mmol) was weighed out and added to a flask with a magnetic stir bar. This was suspended in 11 mL POCl3 and the reaction was heated at reflux for 3 hours. This was evaporated, then quenched with cold 10% aqueous Na2CO3. The mixture was extracted 4 times with ethyl acetate and the combined organic layer was dried over sodium sulfate. This was filtered, concentrated onto a plug of silica, and purified by column chromatography. Pure product was concentrated and dried on the high vacuum to give 493 mg of 5-(4,5-dichloropyrimidin-2-ylamino)-2-cyclopropylbenzonitrile (80% yield, accounting for the mass of p-toluenesulfonic acid present in the starting material).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09062068B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-8e278dfd62b44c2489f7eb17d1b2436f |
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| Source note | uspto-grants-2015_06 |
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