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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81491Generated: October 30, 2026

1-Hydroxybenzotriazole → 3-Amino-5-methyl-pyrazin-2-carboxylic acid methoxy-methyl-amide

https://huagongshe.com/reaction/81491

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Amino-5-methylpyrazine-2-carboxylic acidHCID 279233—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN,O-dimethoxyhydroxylamine hydrochlorideHCID 22015712—
SolventDimethylformamideHCID 6228—
Product3-Amino-5-methyl-pyrazin-2-carboxylic acid methoxy-methyl-amideHCID 86669772—

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Amino-5-methyl-pyrazin-2-carboxylic acid (0.48 g, 3.12 mmol) is dissolved in anhydrous DMF (10 ml) under N2. The brown solution is cooled to 0° C., and diisopropylethylamine (1.48 ml, 7.9 mmol), EDC.HCl (0.75 g, 3.8 mmol), HOBt (0.58 g, 3.8 mmol) and N,O-dimethoxyhydroxylamine hydrochloride (0.37 g, 3.8 mmol) are added and the reaction is stirred at 0° C. for 1 hour and at room temperature for 4 hours. The solvent is concentrated in vacuo, and the residue is diluted with EtOAc and aq. NaHCO3. The phases are separated and the aqueous layer washed with EtOAc. The organic layers are combined, washed with brine, dried (MgSO4) and concentrated in vacuo. Purification by flash chromatography (SiO2, 0-5% MeOH in DCM) yields 3-amino-5-methyl-pyrazin-2-carboylic acid methoxy-methyl-amide as a pale yellow solid. [M+H]+ 197.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846687B2
Source datasetuspto-grants-2014_09
ORD IDord-f78b54efc47940d9b0ae99b22287dd82
Source noteuspto-grants-2014_09