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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415856Generated: October 25, 2026

2-Methoxyethylamine → HCID 178495985, compound

https://huagongshe.com/reaction/415856

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, 1H), 6.27 (s, 2H), 6.10 (t, J=6.5 Hz, 1H), 3.50 (m, 2H), 3.35 (d, J=5.8 Hz, 2H), 3.08 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088803B2
Source datasetuspto-grants-2012_01
ORD IDord-6a8296a7e88f4a6391d02e274b538e8d
Source noteuspto-grants-2012_01