HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724371Generated: October 31, 2026
HCID 21877263, compound → HCID 21877604, compound
https://huagongshe.com/reaction/724371
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 21877263 | HCID 21877263 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetralin | HCID 8404 | — |
| Product | HCID 21877604 | HCID 21877604 | 55% |
Reaction Steps
A suspension of 3-(E-styryl)-6-phenoxy-4,5-dihydro-1H-indazole (200 mg. 0.64 mmol) and 5% Pd/C (200 mg) in 10 mL of tetralin was heated at 155° C. for 18 h. The catalyst was removed by filtering the hot solution and washed with THF, EtOAc and MeOH. The filtrate was concentrated under reduced pressure and the residue was chromatographed on silica gel eluting hexanes/EtOAc (2:1) to provide 3-(E-styryl)-6-phenoxy-1H-indazole as an off-white solid (110 mg, 55%). 1H NMR (DMSO-d6) δ 6.96 (s, 2H), 7.10 (d, 2H, J=7.7 Hz), 7.20 (t, 1H, J=7.1 Hz), 7.30 (t, 1H, J=7.1 Hz), 7.44 (m, 6H), 7.71 (d, 2H, J=7.5 Hz), 8.20 (d, 1H, J=9.2 Hz), 12.90 (s, 1H). Anal. Calc. for C21H16N2O.0.1H2O: C, 80.28; H, 5.20; N, 8.92. Found: C, 80.20; H, 5.21; N, 8.93.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07141587B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-2ae6df201b0045b284e4cad8485250a2 |
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| Source note | uspto-grants-2006_11 |
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