HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224291Generated: October 31, 2026
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 59716583, compound
https://huagongshe.com/reaction/2224291
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | HCID 59716562 | HCID 59716562 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59716583 | HCID 59716583 | 84% |
Reaction Steps
To a solution of 2-(4-(trifluoromethyl)benzyl)-7,8-bis(4-chlorophenyl)-6-methyl-5,6-dihydro-[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-one (28 mg, 0.053 mmol), prepared as described in Example 469 in CH2Cl2 (0.5 mL) at RT was added DDQ (15 mg, 0.064 mmol). The reaction was stirred at RT for 1 h. LC-MS showed the completion of the reaction. The reaction mixture was concentrated under reduced pressure. The resulting residue was purified by using silica gel column chromatography using an automated system eluting with a gradient of (0% to 80% EtOAc for 20 min.) to give the title compound, 2-(4-(trifluoromethyl)benzyl)-7,8-bis(4-chlorophenyl)-6-methyl-[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-one (23 mg, 84% yield) as a yellow solid in 84% yield. HPLC retention time: 4.18 min; MS [M+H]+: found 529. 1H NMR (CDCl3, 400 MHz) δ 7.61 (d, 2H), 7.52 (d, 2H), 7.35 (dd, 2H), 7.27 (dd, 2H), 7.16 (dd, 2H), 7.02 (dd, 2H), 5.28 (s, 2H), 2.29 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07378418B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-f5d05a89ba554b67978ce727bf573c17 |
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| Source note | uspto-grants-2008_05 |
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