HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75171Generated: October 30, 2026
Thioacetamide → 1,2-Diethyl 4-(aminothioxomethyl)tetrahydro-1,2-pyridazinedicarboxylate
https://huagongshe.com/reaction/75171
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thioacetamide | HCID 2723949 | — |
| Reactant | 1,2-Diethyl 4-cyanotetrahydro-1,2-pyridazinedicarboxylate | HCID 71073783 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 1,2-Diethyl 4-(aminothioxomethyl)tetrahydro-1,2-pyridazinedicarboxylate | HCID 86674464 | — |
Reaction Steps
A mixture of 1,2-diethyl 4-cyanotetrahydro-1,2-pyridazinedicarboxylate (i.e the product of Step E) (5.5 g, 0.024 mol) and thioacetamide (5.5 g, 0.073 mol) in trifluoroacetic acid (about 10 mL) was heated at 50° C. for 20 h. The reaction mixture was cooled, and then partitioned between water and diethyl ether (about 30 mL). The layers were separated and the aqueous layer was extracted with diethyl ether (2×). The combined organic extracts were washed with water (about 30 mL), dried magnesium sulfate, filtered and concentrated under reduce pressure to an orange oil. The oil was adsorbed onto Celite® (diatomaceous filter aid), and then purified by silica gel column chromatography (25% to 60% gradient of ethyl acetate in petroleum ether as eluant) to provide the title compound as a yellow solid (3.97 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835427B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-773be965097747278da923c4f415f9ce |
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| Source note | uspto-grants-2014_09 |
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