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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346507Generated: October 30, 2026

Sulfuric Acid → HCID 23057945, compound

https://huagongshe.com/reaction/346507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium BromideHCID 253881—
Reactant4-[6-(Piperidin-1-yl)[1,2,4]triazolo[4,3-b]pyridazin-3-yl]-1,3-thiazol-2-amineHCID 23057950—
ReactantSodium NitriteHCID 23668193—
CatalystCopper SulfateHCID 24462—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventChloroformHCID 6212—
ProductHCID 23057945HCID 230579456.9%

Reaction Conditions

Temperature-5 °C

Reaction Steps

A solution mixture of concentrated sulfuric acid (1.5 ml) and water (3 ml) was cooled to −5° C., and 4-(6-piperidin-1-yl-1,2,4-triazolo[4,3-b]pyridazin-3-yl)-1,3-thiazol-2-amine (0.90 g), copper (II) sulfate (1.50 g) and sodium bromide (0.62 g) were added successively, and the mixture was stirred at 0° C. for 5 minutes. Then, a solution of sodium nitrite (0.25 g) in water (1.6 ml), followed by stirring at room temperature overnight. The reaction solution was combined with water, chloroform and 2-propanol, and insoluble materials were filtered off. The resultant organic phase was washed with water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The resultant residue was purified by silica gel column chromatography (eluent: chloroform:methanol=20:1) to obtain crude crystals, which were then recrystallized from ethanol-diethyl ether to obtain 3-(2-bromo-1,3-thiazol-4-yl)-6-piperidin-1-yl-1,2,4-triazolo[4,3-b]pyridazine (75 mg) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173033B2
Source datasetuspto-grants-2007_02
ORD IDord-d4b42c9368c848eda00c76dc5d153552
Source noteuspto-grants-2007_02