HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923351Generated: November 1, 2026
p-Toluenesulfonic acid → HCID 178515498, compound
https://huagongshe.com/reaction/923351
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 178472159 | HCID 178472159 | — |
| Reactant | HCID 178508279 | HCID 178508279 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 178515498 | HCID 178515498 | — |
Reaction Steps
A mixture of 3-(2-chlorophenyl)-1H-1,2,4-triazol-5-amine (50 mg, 0.26 mmol, 1.00 equiv), ethyl 3-(1H-1,2,3-benzotriazol-5-yl)-3-oxopropanoate (100 mg, 0.43 mmol, 1.67 equiv), butan-1-ol (1 mL), and p-TsOH (5 mg, 0.03 mmol, 0.11 equiv) was stirred for 1 h at 170° C. in an oil bath. After the reaction was completed, the solids were collected by filtration and washed with MeOH (3×1 ml). This resulted in 25.3 mg (27%) of 5-(1H-benzo[d][1,2,3]triazol-6-yl)-2-(2-chlorophenyl)-[1,2,4]triazolo[1,5-c]pyrimidin-7(4H)-one as a grey solid.
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-88ca8918442142fe91ce0e4c37db929f |
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| Source note | uspto-grants-2016_03 |
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