Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674878Generated: November 1, 2026

p-tert-Butoxybenzaldehyde → HCID 67342633, compound

https://huagongshe.com/reaction/1674878

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-tert-ButoxybenzaldehydeHCID 93774—
Reactant6-Piperazino-3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazineHCID 1476862—
ProductHCID 67342633HCID 67342633—

Reaction Steps

Reductive amination of 6-(piperazin-1-yl)-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazine with 4-[(2-methylpropan-2-yl)oxy]benzaldehyde was carried out according to General Synthetic Method 7. The crude product was purified by hplc using a Waters XBridge Prep C18 OBD column, 5μ silica, 30 mm diameter, 100 mm length eluted with decreasingly polar mixtures of water (containing 0.1% aqueous ammonia) and acetonitrile as eluents to give 6-[4-[[4-[(2-methylpropan-2-yl)oxy]phenyl]methyl]piperazin-1-yl]-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003649B2
Source datasetuspto-grants-2011_08
ORD IDord-0314ce00a0934a7d9aeed2abd943b615
Source noteuspto-grants-2011_08