HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715728Generated: October 31, 2026
Thiophene-2-carbohydrazide → HCID 5310124, compound
https://huagongshe.com/reaction/715728
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thiophene-2-carbohydrazide | HCID 73098 | — |
| Reactant | HCID 86701044 | HCID 86701044 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 5310124 | HCID 5310124 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187484B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-0cce792853a84361810a32f39a3a735e |
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| Source note | uspto-grants-2015_11 |
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