HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923340Generated: October 29, 2026
p-Toluenesulfonic acid → HCID 178515487, compound
https://huagongshe.com/reaction/923340
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Ethyl 3-(2H-1,3-benzodioxol-5-yl)-3-oxopropanoate | HCID 2756586 | — |
| Reactant | HCID 178508293 | HCID 178508293 | — |
| Solvent | Diphenyl Ether | HCID 7583 | — |
| Product | HCID 178515487 | HCID 178515487 | 24.2% |
Reaction Steps
To a solution of 3-(4-chlorophenyl)-1H-1,2,4-triazol-5-amine (50 mg, 0.26 mmol) in diphenyether (2 ml) was added TsOH (2.2 mg, 0.01 mmol) and ethyl 3-(benzo[d][1,3]dioxol-5-yl)-3-oxopropanoate (81 mg, 0.34 mmol). After stirring 2 h at 170° C., the reaction was quenched by the addition of hexane (5 ml), the product was collected by filtration and washed with methanol (10 ml) and dried in an oven under reduced pressure to give 5-(benzo[d][1,3]dioxol-5-yl)-2-(4-chlorophenyl)-[1,2,4]triazolo[1,5-α]pyrimidin-7(4H)-one as a off-white solid (23.1 mg, 24%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278973B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-30ae433dc90c4542a6920ffa4431b565 |
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| Source note | uspto-grants-2016_03 |
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