HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154038Generated: October 31, 2026
HCID 20435938, compound → HCID 20435958, compound
https://huagongshe.com/reaction/1154038
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 20435938 | HCID 20435938 | — |
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 20435958 | HCID 20435958 | — |
Reaction Steps
A mixture of 6.43 g (17 mmol) of methyl 2,3,5,8-tetrahydro-2-(2-iodoethyl)-2-methyl-1,3-dioxo-1H-pyrazolo-[1,2-a]pyridazine-5-carboxylate and 1.94 g (17 mmol) of potassium thioacetate in 150 ml of acetone was stirred at room temperature for 5 hours. The solvent was removed by evaporation and the residue was partitioned between dichloromethane and water. The organic phase was separated, dried over magnesium sulfate and evaporated to give methyl 2-(2-acetylthioethyl)-2,3,5,8-tetrahydro-2-methyl-1,3-dioxo-1H-pyrazolo[1,2-a]pyridazine-5-carboxylate as a mixture of diastereomers. Chromatography on silica gel using diethyl ether for the elution gave 3.81 g (69%) of diastereomer A in the form of a colorless oil and 1.26 g (23%) of diastereomer B in the form of a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04487929 |
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| Source dataset | uspto-grants-1984_12 |
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| ORD ID | ord-83365bed99c5426eb7831fa2567c86a2 |
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| Source note | uspto-grants-1984_12 |
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