HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2282157Generated: October 31, 2026
Tetrahydrofuran → 2-Aminopyridine-4-carbothioamide
https://huagongshe.com/reaction/2282157
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Diethyl dithiophosphate, potassium salt | HCID 1385274 | — |
| Reactant | 2-Aminoisonicotinonitrile | HCID 7015524 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Aminopyridine-4-carbothioamide | HCID 24693836 | 81% |
Reaction Steps
A mixture of 2-aminopyridine-4-carbonitrile (6.0 g, 50 mmol), O,O′-diethyl dithiophosphate (11 mL, 60 mmol), tetrahydrofuran (25 mL) and water (25 mL) was stirred at 60° C. for 4 hr. To the reaction mixture was added O,O′-diethyl dithiophosphate (2.8 mL, 15 mmol) and the mixture was stirred at 60° C. for 1 day. To the reaction mixture was added aqueous sodium bicarbonate solution, and the mixture was extracted with ethyl acetate. The combined organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, and the insoluble material was filtered off. The filtrate was concentrated under reduced pressure, and the obtained residue was washed with diisopropyl ether to give the title compound (6.2 g, 81%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09139589B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-b6ca5242bd964e52875f2137b1e320ce |
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| Source note | uspto-grants-2015_09 |
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