HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253394Generated: October 26, 2026
1,2-Diaminocyclohexane → N4-(2-Ethylpyrazolo[1,5-a]pyridin-3-yl)tetrahydro-2H-4-pyrancarboxamide
https://huagongshe.com/reaction/2253394
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Diaminocyclohexane | HCID 4610 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Oxane-4-carboxamide | HCID 13197203 | — |
| Reactant | 2-Ethyl-3-iodopyrazolo[1,5-a]pyridine | HCID 16114933 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | N4-(2-Ethylpyrazolo[1,5-a]pyridin-3-yl)tetrahydro-2H-4-pyrancarboxamide | HCID 21084121 | 79.6% |
Reaction Steps
A mixture of 2-ethyl-3-iodopyrazolo[1,5-a]pyridine (350 g, 1.29 mol), tetrahydro-2H-4-pyrancarboxamide (249 g, 1.93 mol), copper iodide (49.0 g, 258 mmol), tripotassium phosphate (hydrate) (546 g, 2.57 mol), 1,2-cyclohexanediamine (mixture of cis and trans) (58.7 g, 514 mmol) and xylene (3500 mL) was stirred while heating at an external temperature of 120° C. (oil bath). The reaction mixture was heated and stirred for 6 hours, and then heating was terminated and upon reaching an internal temperature of 61.5° C., hot water (58° C., 3500 mL) was added to the reaction mixture and stirring was continued overnight. After adding 28% aqueous ammonia (1050 mL) to the reaction mixture and stirring for 1 hour, the precipitate was filtered out and washed with water (1750 mL) and ethyl acetate (1050 mL) and then dried under aeration at 60° C. overnight to afford 280 g of the title compound (major conformer:minor conformer=6:1) (79.6% yield)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07323569B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-1194045c4b864185a2bd2356a0a32c28 |
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| Source note | uspto-grants-2008_01 |
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