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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356420Generated: October 26, 2026

Lipoic acid → 5-[1,2]DITHIOLAN-3-YL-PENTANOIC Acid {6-[4-(2-TRIFLUOROMETHYLBENZOYL)PIPERAZIN-1-YL]PYRIDAZIN-3-YL}AMIDE

https://huagongshe.com/reaction/2356420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLipoic acidHCID 6112—
Reactant[4-(6-Aminopyridazin-3-yl)piperazin-1-yl](2-trifluoromethylphenyl)methanoneHCID 66849536—
Product5-[1,2]DITHIOLAN-3-YL-PENTANOIC Acid {6-[4-(2-TRIFLUOROMETHYLBENZOYL)PIPERAZIN-1-YL]PYRIDAZIN-3-YL}AMIDEHCID 86597210—

Reaction Steps

Following the procedure of Example 2, making variations only as required to use lipoic acid in place of benzyloxyacetic acid to react with [4-(6-aminopyridazin-3-yl)piperazin-1-yl](2-trifluoromethylphenyl)methanone, the title compound was obtained as a white solid (yield 8%). 1H NMR (300 MHz, CDCl3) δ 10.11, 8.37, 7.72, 7.61, 7.53, 7.35, 7.04, 4.08-3.84, 3.70-3.57, 3.56-3.46, 3.33-3.30, 3.17-3.02, 2.59, 2.39, 1.84, 1.78-1.56, 1.51-1.37. 13C NMR (300 MHz, CDCl3): 172.52, 167.57, 157.94, 150.00, 134.42, 132.38, 129.45, 127.79, 127.29, 127.14, 126.93, 126.88, 126.82, 121.92, 116.27, 56.34, 46.47, 45.65, 45.33, 41.25, 40.26, 38.49, 37.05, 34.74, 28.85, 25.14. MS (ES+) m/z 540.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759348B2
Source datasetuspto-grants-2010_07
ORD IDord-6f7e8258b13e423a8c3b2f490d59a728
Source noteuspto-grants-2010_07