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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258153Generated: November 1, 2026

4-(Trifluoromethyl)benzaldehyde → HCID 59253662, compound

https://huagongshe.com/reaction/1258153

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)benzaldehydeHCID 67996—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 59253661HCID 59253661—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 59253662HCID 5925366239.9%

Reaction Steps

To a mixture of 6-(piperidin-4-ylamino)-pyridazine-3-carbonitrile (D3) (0.15 g, 0.7 mmol) and α,α,α-trifluoro-p-tolualdehyde (0.15 ml, 1.1 mmol) in dichloromethane (2 ml), was added sodium triacetoxyborohydride (0.232 g, 1.1 mmol) and acetic acid (0.041 ml). The reaction mixture was then stirred at room temperature for 18 h. A saturated solution of sodium hydrogen carbonate was then added and the organic layer was separated, dried (Na2SO4), filtered and the solvent evaporated in vacuo. The residue was purified by HPLC. The desired fractions were collected and the solvent was evaporated in vacuo to yield E7 (0.101 g, 38%) as a solid. C18H18F3N5 requires 361. Found 362 (MH+); mp: 243.1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466153B2
Source datasetuspto-grants-2013_06
ORD IDord-68f03510272b4d7c8d032d30853a599b
Source noteuspto-grants-2013_06