HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005678Generated: November 1, 2026
Phosphorus oxychloride → HCID 22674092, compound
https://huagongshe.com/reaction/1005678
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 22674130 | HCID 22674130 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 22674092 | HCID 22674092 | 49.4% |
Reaction Steps
In chloroform (100 ml) was dissolved 3.0 g of 6-(4-toluenesulfonylamino)isoquinoline (Preparation Example 21), and m-chloroperbenzoic acid (2.57 g) was added thereto under ice-cooling, followed by stirring at room temperature overnight. The solvent was evaporated, and the resulting crystals were washed with diethyl ether, collected by filtration and dried, to give pale yellow crystals. The obtained crystals were suspended in chloroform (83 ml), and phosphorus oxychloride (19 ml) was added thereto, followed by heating under reflux for 5 hours. After cooling, the solvent was evaporated, and the residue was basified with an aquesou sodium bicarbonate in an ice-bath, followed by extracting with ethyl acetate, The extract was washed with brine, dried over anhydrous magnesium sulfate and the solvent was evaporated. The residue was purified by silica gel column, to give crude crystals of the title compound (1.630 g, 49.40%). The crude crysatals were recrystallized from ethanol, to give the title compound as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06787534B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-7a63818d78584ea8903c0fe8b35f5602 |
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| Source note | uspto-grants-2004_09 |
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