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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514383Generated: November 4, 2026

Sodium Carbonate → Racemic (4,4-difluorocyclohexyl)(trans-2,5-dimethyl-4-(1-phenylpyrido[3,4-d]pyridazin-4-yl)piperazin-1-yl)methanone

https://huagongshe.com/reaction/1514383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantHOAtHCID 181649—
Reactant4,4-Difluorocyclohexanecarboxylic acidHCID 2779136—
ReactantRacemic 4-(trans-2,5-dimethylpiperazine-1-yl)-1-phenylpyrido[3,4-d]pyridazineHCID 68796083—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductRacemic (4,4-difluorocyclohexyl)(trans-2,5-dimethyl-4-(1-phenylpyrido[3,4-d]pyridazin-4-yl)piperazin-1-yl)methanoneHCID 25227134—

Reaction Steps

To racemic trans 4-(2,5-dimethylpiperazine-1-yl)-1-phenylpyrido[3,4-d]pyridazine 44 (360 mg, 1127 μmol) dissolved in 4 mL of DMF was added EDCI (259 mg, 1.35 mmol), 4,4-difluorocyclohexanecarboxylic acid (204 mg, 1.24 mmol), 3H-[1,2,3]triazolo[4,5-b]pyridin-3-ol (184 mg, 1.35 mmol) (HOAT), and sodium carbonate (239 mg, 2.25 mmol). The reaction was stirred at RT for 4 h, and the solvent was removed in vacuo. The crude reaction mixture was dissolved in 100 mL of ethyl acetate and washed with 1×25 mL of water, 1×25 mL of sat. NaHCO3, and 1×25 mL of brine. The organic layer was dried over MgSO4, filtered, and concentrated. Purified by column chromatography to isolate racemic (4,4-difluorocyclohexyl)(trans-2,5-dimethyl-4-(1-phenylpyrido[3,4-d]pyridazin-4-yl)piperazin-1-yl)methanone 45. MS 465.2 (calc'd) 466.1 (M+H, found).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222251B2
Source datasetuspto-grants-2012_07
ORD IDord-2318a1ec2cac4411acaa94837c130da5
Source noteuspto-grants-2012_07