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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381077Generated: November 1, 2026

Indole → HCID 46893454, compound

https://huagongshe.com/reaction/2381077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 68502134HCID 68502134—
SolventMethanolHCID 887—
ProductHCID 46893454HCID 4689345440%

Reaction Conditions

Temperature65 °C

Reaction Steps

Potassium hydroxide (156 mg, 2.79 mmol) was added to 1-[3-(trifluoromethyl)-7,8-dihydro-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperidin-4-one (200 mg, 0.70 mmol) and 1H-indole (90 mg, 0.77 mmol) in MeOH (3 mL). The resulting mixture was stirred at 65° C. for 20 hours. The reaction mixture was evaporated to dryness then quenched with saturated aqueous ammonium chloride (0.5 mL), diluted with water (50 mL) and extracted with ethyl acetate (2×50 mL). The combined organic layers were washed with saturated brine (25 mL), dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 5% MeOH in DCM. Pure fractions were evaporated to dryness to afford 6-[4-(1H-indol-3-yl)-5,6-dihydropyridin-1(2H)-yl]-3-(trifluoromethyl)-7,8-dihydro-[1,2,4]triazolo[4,3-b]pyridazine (107 mg, 40%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258140B2
Source datasetuspto-grants-2012_09
ORD IDord-9196cac2617c45039d9e1ea3f7559e17
Source noteuspto-grants-2012_09