HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74222Generated: October 29, 2026
2-Methoxyethylamine → 2-(2-(2-Methoxyethyl)aminoanilin-5-yl)benzoxazole
https://huagongshe.com/reaction/74222
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methoxyethylamine | HCID 8018 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(4-Fluoro-3-nitrophenyl)benzoxazole | HCID 21990970 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-(2-Methoxyethyl)aminoanilin-5-yl)benzoxazole | HCID 67499198 | 31% |
Reaction Steps
To a suspension of 2-(4-fluoro-3-nitrophenyl)benzoxazole (see Working Example 15-2) (300 mg, 1.16 mmol) in ethanol (5 mL) was added potassium carbonate (176 mg, 1.28 mmol) and 2-methoxyethylamine (105 mg, 1.39 mmol), and this was heated to reflux for 3.5 hours. After the reaction was complete, this was cooled to room temperature, water was added, and the precipitated crystals were filtered, washed with water and then dried. To a tetrahydrofuran solution (7 mL) of the crystals obtained was added 10% palladium-carbon (100 mg). A hydrogen atmosphere was substituted in the flask, and this was stirred at room temperature for 6 hours. After the reaction was complete, this was filtered through Celite and the filtrate was concentrated. The residue obtained was purified by silica gel column chromatography to yield the title compound (102 mg, 31% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829035B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-fbad706f2d1b47cf908192501dd2aaac |
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| Source note | uspto-grants-2014_09 |
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