HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530677Generated: November 3, 2026
p-Toluenesulfonic acid → HCID 68312923, compound
https://huagongshe.com/reaction/1530677
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 68313110 | HCID 68313110 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 68312923 | HCID 68312923 | 91% |
Reaction Steps
A mixture of 12-(1-ethoxyethenyl)-4-[1-(2-methoxypropyl)-1H-1,2,4-triazol-5-yl]-9-oxa-3,6-diazatricyclo[8.4.0.02,6]tetradeca-1(14),2,4,10,12-pentaene (190 mg, 0.480 mmol) and p-toluenesulfonic acid (11 mg, 0.060 mmol) in acetone (10 mL) was stirred at 60° C. for 75 min. The solid was filtered off and the filtrate was concentrated. The residue was purified by reverse phase Combiflash eluting with a 0-40% gradient of CH3CN in 0.3% NH4HCO3 to afford 1-{4-[1-(2-methoxypropyl)-1H-1,2,4-triazol-5-yl]-9-oxa-3,6-diazatricyclo[8.4.0.02,6]tetradeca1(14),2,4,10,12-pentaen-12-yl}ethan-1-one (160 mg, 91% yield). LCMS (ESI) m/z: 368.1 [M+H+]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09090628B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-a9464f4c2dae4b8ba6127f98be2c7730 |
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| Source note | uspto-grants-2015_07 |
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