HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173120Generated: November 3, 2026
Phosphorus oxychloride → HCID 22674092, compound
https://huagongshe.com/reaction/1173120
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
6-(4-Toluenesulfonylamino) isoquinoline (3.0 g, Production Example 21b) was dissolved in chloroform (100 ml). Under ice-cooling, m-chloroperbenzoic acid (2.57 g) was added thereto, 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 crystals were suspended in chloroform (83 ml) and phosphorous oxychloride (19 ml) was added thereto, followed by heating under reflux for 5 hours. After cooling, the solvent was evaporated. The residue was basified by adding an aqueous saturated sodium bicarbonate in an ice bath, and then the mixture was extracted with ethyl acetate. The extract was washed with brine and 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 crystals 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 | US07834049B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-7ee22318b0f94471ba67c7a764b9271f |
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| Source note | uspto-grants-2010_11 |
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