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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674866Generated: October 26, 2026

1,3-Benzodioxole-4-carboxaldehyde → 6-[4-(1,3-Benzodioxol-4-ylmethyl)piperazin-1-yl]-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazine

https://huagongshe.com/reaction/1674866

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Benzodioxole-4-carboxaldehydeHCID 82264—
Reactant6-Piperazino-3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazineHCID 1476862—
Product6-[4-(1,3-Benzodioxol-4-ylmethyl)piperazin-1-yl]-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazineHCID 67340023—

Reaction Steps

Reductive amination of 6-(piperazin-1-yl)-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazine with 1,3-benzodioxole-4-carbaldehyde 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, 21 mm diameter, 100 mm length eluted with decreasingly polar mixtures of water (containing 0.05% aqueous ammonia) and acetonitrile as eluents to give 6-[4-(1,3-benzodioxol-4-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-bf3ca79927fe4ac188dd55eb6512ced6
Source noteuspto-grants-2011_08