HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893708Generated: October 30, 2026
Sodium Hydroxide → 5-Ethynyl-1H-imidazole-4-carboxamide
https://huagongshe.com/reaction/893708
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Ethynyl-1-pentofuranosyl-1H-imidazole-4-carboximidic acid | HCID 453180 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 5-Ethynyl-1H-imidazole-4-carboxamide | HCID 14886843 | 37.6% |
Reaction Steps
A solution of 200 mg (0.75 mmol) of 5-ethynyl-1-β-D-ribofuranosylimidazole-4-carboxamide in 5 ml of 1N hydrochloric acid solution was heated under reflux at 100° C. for 4 hours. After the reaction, the reaction solution was neutralized with 1N sodium hydroxide solution, silica gel powder was added, and the solvent was evaporated. The residue was adsorbed onto a silica gel column (2.7×11 cm), eluted with a 0-16% ethanolchloroform solvent mixture, and crystallized from an ethanol-hexane solvent mixture to obtain 38 mg of pale yellow crystals of 5-ethynylimidazole-4-carboxamide (yield: 37.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05126361 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-52527abc49d54b6f8006a947a02b2d05 |
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| Source note | uspto-grants-1992_06 |
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