HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69812Generated: October 25, 2026
2-Methoxyethylamine → HCID 178495985, compound
https://huagongshe.com/reaction/69812
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methoxyethylamine | HCID 8018 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (Z)-4-amino-N-hydroxy-1,2,5-oxadiazole-3-carbonimidoyl chloride | HCID 4040027 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178495985 | HCID 178495985 | 119% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08822511B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-ae13d21c442e42d3994406751670920b |
|---|
| Source note | uspto-grants-2014_09 |
|---|