HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336668Generated: October 30, 2026
2-Morpholinoethanol → HCID 24957862, compound
https://huagongshe.com/reaction/336668
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Morpholinoethanol | HCID 61163 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | HCID 135907847 | HCID 135907847 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 24957862 | HCID 24957862 | 63.9% |
Reaction Steps
To a solution of 4-(6,8-dimethoxyisoquinolin-3-yl)-2,6-dimethylphenol (0.309 g, 1.0 mol) in anhydrous THF (20 mL), triphenyl phosphene (0.52 g, 2.0 mmol), 4-(2-hydroxyethyl)morpholine (0.262 g, 2.0 mmol) and N,N-diisopropylethylamine (0.387 g, 3.0 mmol) were added. To this stirred solution was added diethylazodicarboxylate (0.348 g, 2.0 mmol). The reaction mixture was stirred at room temperature overnight under nitrogen, then diluted with ethyl acetate (100 mL). The organic layer was washed with water and brine, and dried over anhydrous Na2SO4. The solvent was removed under reduced pressure. The crude material was purified by column chromatography to give 3-[3,5-dimethyl-4-(2-morpholin-4-ylethoxy)phenyl]-6,8-dimethoxyisoquinoline (0.54 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889698B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-1da72e9fdcbe41cc8330a347f9ba310f |
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| Source note | uspto-grants-2014_11 |
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