HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 619951Generated: October 30, 2026
Phosphorus oxychloride → HCID 15017543, compound
https://huagongshe.com/reaction/619951
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178429186 | HCID 178429186 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 15017543 | HCID 15017543 | — |
Reaction Steps
Phosphorus oxychloride (135 ml, 1.47 mol) was diluted with 335 ml of dry acetonitrile and added to 15 g (40 mmol) of N-(2-trifluoromethylphenyl)-7-hydroxy-5-methyl-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamide in a one liter flask and heated to reflux with stirring. After about 3 days, the reaction was found to be complete by thin layer chromatography. Volatiles were removed by evaporation under reduced pressure until the mixture became very viscous and the residue was poured onto about one liter of ice and water with stirring. After about 30 minutes, the solid that formed was collected by filtration, washed with ice water, and dried under reduced pressure at room temperature. It was then dissolved in methylene chloride and the resulting solution dried over magnesium sulfate for about five minutes and filtered. The volatiles were removed from the filtrate by evaporation under reduced pressure to obtain the title compound as a white solid residue. The product, the structure of which was confirmed by NMR analysis, amounted to 13.4 g (85.4 percent of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04818273 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-124ec0ecb74346dcaff4e61fa48ddaac |
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| Source note | uspto-grants-1989_04 |
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