HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154039Generated: October 28, 2026
HCID 13144528, compound → HCID 13144530, compound
https://huagongshe.com/reaction/1154039
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 13144528 | HCID 13144528 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 13144530 | HCID 13144530 | 43% |
Reaction Steps
A solution of 0.71 g of tert.butyl 2-acetylthiomethyl-hexahydro-2-methyl1,3-dioxo-1H-pyrazolo[1,2-a]pyridazine-5-carboxylate (diastereomer A) in 10 ml of trifluoroacetic acid was left to stand at room temperature for 1 hour. The mixture was evaporated to dryness and the residue was stirred under nitrogen with 50 ml of 50:50 mixture of water and concentrated aqueous ammonia for 2 hours. The mixture was acified to pH 1 with hydrochloric acid, saturated with sodium chloride and extracted with chloroform. The chloroform extracts were dried over sodium sulfate and evaporated. The residue was recrystallized from ethyl acetate/hexane to give 0.22 g (43%) of hexahydro-2-mercaptomethyl-2-methyl-1,3-dioxo-1H-pyrazolo[1,2-a]pyridazine-5-carboxylic acid (diastereomer A) in the form of white crystals having a melting point of 209°-211° C.
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-f0a5c346f7084b82b686ea2488ff5470 |
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| Source note | uspto-grants-1984_12 |
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