HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828203Generated: November 1, 2026
2-Methoxyethylamine → HCID 22063892, compound
https://huagongshe.com/reaction/1828203
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methoxyethylamine | HCID 8018 | — |
| Reactant | HCID 86587987 | HCID 86587987 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 22063892 | HCID 22063892 | — |
Reaction Steps
To a benzene (3 mL) solution of [4-(1,3-Diethyl-2-oxo-2,3-dihydro-1H-benzoimidazol-5-yl)-3-m-tolyl-pyrazol-1-yl]-acetaldehyde (0.034 g) was added methoxyethylamine (0.03 mL) and 4 Å molecular sieves. The reaction was allowed to stand at 23° C. for 1 hour then was filtered and concentrated. The resulting oil was diluted with methanol (2 mL), 4 Å molecular sieves were added and the mixture was treated with sodium cyanoborohydride (0.02 g). After stirring for 18 hours the mixture was poured onto ethyl acetate/saturated sodium bicarbonate and extracted. The organic layer was dried over sodium sulfate and concentrated. Preparative thin layer chromatography gave 1,3-Diethyl-5-{1-[2-(2-methoxy-ethylamino)-ethyl]-3-m-tolyl-1H-pyrazol-4-yl}-1,3-dihydro-benzoimidazol-2-one (0.014 g). Subsequent treatment with 1M hydrochloric acid in ether gave the hydrochloride salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07056918B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-de977f1a1af5421a88e3cda9152ba99f |
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| Source note | uspto-grants-2006_06 |
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