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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715728Generated: October 31, 2026

Thiophene-2-carbohydrazide → HCID 5310124, compound

https://huagongshe.com/reaction/715728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophene-2-carbohydrazideHCID 73098—
ReactantHCID 86701044HCID 86701044—
Solvent1-ButanolHCID 263—
ProductHCID 5310124HCID 5310124—

Reaction Conditions

Temperature142.5 °C

Reaction Steps

To 2-thiophenecarbohydrazide (215 mg, 1.5 mmol) dissolved in n-BuOH (3 mL) was added ethyl 2-((6-chloropyridazin-3-yl)thio)propanoate (232 mg, 1 mmol), and the whole was heated for 5 h in a 140-145° C. oil bath. The reaction mixture was then cooled to room temperature (˜25° C.), and the solid residue removed by filtration. The filtrate was then diluted with methylene chloride (50 mL), and washed with saturated with NaHCO3 (˜15 mL). The combined aqueous layers were washed twice with methylene chloride, and the organic layers were then combined, washed with brine, dried over MgSO4, filtered, and evaporated. The resulting solid was then recrystallized from EtOH to give ethyl 2-((3-(thiophen-2-yl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)thio)acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187484B2
Source datasetuspto-grants-2015_11
ORD IDord-0cce792853a84361810a32f39a3a735e
Source noteuspto-grants-2015_11