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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674850Generated: October 30, 2026

3-Thiophenecarboxaldehyde → HCID 17407764, compound

https://huagongshe.com/reaction/1674850

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ThiophenecarboxaldehydeHCID 68135—
Reactant6-Piperazino-3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazineHCID 1476862—
ProductHCID 17407764HCID 17407764—

Reaction Steps

Reductive amination of 6-(piperazin-1-yl)-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazine with thiophene-3-carbaldehyde was carried out according to General Synthetic Method 5. The crude product was purified by hplc using a Waters XBridge Prep C18 OBD column (5μ silica, 19 mm diameter, 100 mm length) eluted with decreasingly polar mixtures of water (containing 1% aqueous ammonia) and acetonitrile as eluents to give 6-[4-(thiophen-3-ylmethyl)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-5839550a1d0c4e77bbda08adc330113d
Source noteuspto-grants-2011_08