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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69812Generated: October 25, 2026

2-Methoxyethylamine → HCID 178495985, compound

https://huagongshe.com/reaction/69812

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethylamineHCID 8018—
ReactantTriethylamineHCID 8471—
Reactant(Z)-4-amino-N-hydroxy-1,2,5-oxadiazole-3-carbonimidoyl chlorideHCID 4040027—
SolventEthyl AcetateHCID 8857—
ProductHCID 178495985HCID 178495985119%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

4-Amino-N-hydroxy-1,2,5-oxadiazole-3-carboximidoyl chloride (can be prepared according to Example 1, steps A-B, 200.0 g, 1.23 mol) was mixed with ethyl acetate (1.2 L). At 0-5° C. 2-methoxyethylamine [Aldrich, product #143693] (119.0 mL, 1.35 mol) was added in one portion while stirring. The reaction temperature rose to 41° C. The reaction was cooled to 0-5° C. Triethylamine (258 mL, 1.84 mol) was added. After stirring 5 min, LCMS indicated reaction completion. The reaction solution was washed with water (500 mL) and brine (500 mL), dried over sodium sulfate, and concentrated to give the desired product (294 g, 119%) as a crude dark oil. LCMS for C6H12N5O3 (M+H)+: m/z=202.3. 1H NMR (400 MHz, DMSO-d6): δ 10.65 (s, 1 H), 6.27 (s, 2 H), 6.10 (t, J=6.5 Hz, 1 H), 3.50 (m, 2 H), 3.35 (d, J=5.8 Hz, 2 H), 3.08 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822511B2
Source datasetuspto-grants-2014_09
ORD IDord-ae13d21c442e42d3994406751670920b
Source noteuspto-grants-2014_09