HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415757Generated: October 30, 2026
Triethylamine → n-Hydroxypyrimidine-5-carboximidamide
https://huagongshe.com/reaction/2415757
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Pyrimidine-5-carbonitrile | HCID 10197646 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | n-Hydroxypyrimidine-5-carboximidamide | HCID 34181140 | 52.2% |
Reaction Steps
5-Cyanopyrimidine (J. Org. Chem. 1962, 27, 2264) (0.64 g, 6.1 mmol) was dissolved in methanol (20 mL), the solution was cooled to 0° C. then hydroxylamine hydrochloride (0.42 g, 6.1 mmol) and triethylamine (0.84 mL, 6.1 mmol) were added and the mixture was heated to reflux overnight. The mixture was cooled to room temperature, and the solvent was removed in vacuo. The residue was pre-absorbed onto silica gel, and purified by flash chromatography on silica gel (dichloromethane/methanol/aqueous ammonia—95:5:0.5 as eluant) to give a yellow solid which was contaminated with triethylamine hydrochloride. Recrystallisation from ethanol gave the title compound as a white solid (0.44 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06821972B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-a93ff3a5d7bf4bb0a869ab4bbd72fe5b |
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| Source note | uspto-grants-2004_11 |
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