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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674841Generated: October 28, 2026

Indole-5-carboxaldehyde → HCID 67340539, compound

https://huagongshe.com/reaction/1674841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndole-5-carboxaldehydeHCID 589040—
Reactant6-Piperazino-3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazineHCID 1476862—
ProductHCID 67340539HCID 67340539—

Reaction Steps

Reductive amination of 6-(piperazin-1-yl)-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazine with 1H-indole-5-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-(1H-indol-5-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-daf10010f28a4d60b846fdace0cfecb6
Source noteuspto-grants-2011_08