HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709218Generated: October 31, 2026
Hydrochloric Acid → 1-cyclohexyl--cyanoquinoxaline-2,3(1H,4H)-dione
https://huagongshe.com/reaction/1709218
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-(Cyclohexylamino)-3-nitrobenzonitrile | HCID 2985200 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 1-cyclohexyl--cyanoquinoxaline-2,3(1H,4H)-dione | HCID 53871736 | 25% |
Reaction Steps
A solution of 1.2 g (4.9 mmol N-Cyclohexyl-4-cyano-2-nitroaniline 100 ml ethyl acetate was hydrogenated at 40 psi by using 5% Pd/C (100 mg) as a catalyst. The reaction mixture was filtered and 2.0 g (20 mmol) dry triethylamine was added. A solution of 2.7 g (20 mmol) ethyl oxalyl chloride in 20 ml ethyl acetate was added dropwise and the reaction mixture was stirred for 3 h. The reaction mixture was filtered and evaporated in vacuo to give an oil. A mixture of the oil, 20 ml ethanol and 70 ml 0.5 N hydrochloric acid was refluxed for 1 h. After cooling to 25° C. the precipitate was filtered off and washed with water to give 0.33 g (25 %) 1-cyclohexyl--cyanoquinoxaline-2,3(1H,4H)-dione. M.p.(DSC): decomp. 1H-NMR (DMSO-d6): 12.0 )1H, broad s), 8.0-7.4 (3H, m), 4.4 (1H, m), 2.7-0.7 (10H, m). IR (KBr): 2450, 1700 cm -1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04948794 |
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| Source dataset | uspto-grants-1990_08 |
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| ORD ID | ord-27f6e0ec4d7d4674b630274f9b814c7f |
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| Source note | uspto-grants-1990_08 |
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