HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368432Generated: November 1, 2026
HCID 57435373, compound → HCID 57513765, compound
https://huagongshe.com/reaction/2368432
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 57435373 | HCID 57435373 | — |
| Reactant | HCID 57435374 | HCID 57435374 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 57513765 | HCID 57513765 | — |
Reaction Steps
1-Benzyl-5-(4-fluorophenyl)-1H-1,2,4-triazol-3-amine (4.15 g, 15.47 mmol), 2-(benzyloxy)-4,4-dimethyloxazol-5(4H)-one (4.07 g, 18.56 mmol) were stirred in 5 ml of toluene in a 100 ml prbf. The white suspension was allowed to stir at 50° C. for over weekend. It was then cooled to r.t. The volatiles were removed in vacuo and the resulted solid was dissolved in EtOAc (130 mL) and heptane (50 mL) with heating. It was cooled to r.t. and let sit overnight. The resulted precipitates were collected and dried to afford the title compound. 1H NMR (400 MHz, DMSO-d6) 1.41 (s, 6H) 5.01 (s, 2H) 5.43 (s, 2H) 7.12 (d, J=6.82 Hz, 2H) 7.23-7.43 (m, 11H) 7.64-7.74 (m, 2H), 10.05 (br. s., 1H). MS (m/z) 488.1 M(+1), tR=1.60, Method A.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08703761B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-a2d049a160b546a8a45e00ceb765feab |
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| Source note | uspto-grants-2014_04 |
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