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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415757Generated: October 30, 2026

Triethylamine → n-Hydroxypyrimidine-5-carboximidamide

https://huagongshe.com/reaction/2415757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriethylamine hydrochlorideHCID 11130—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantPyrimidine-5-carbonitrileHCID 10197646—
SolventMethanolHCID 887—
Productn-Hydroxypyrimidine-5-carboximidamideHCID 3418114052.2%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06821972B2
Source datasetuspto-grants-2004_11
ORD IDord-a93ff3a5d7bf4bb0a869ab4bbd72fe5b
Source noteuspto-grants-2004_11