HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388101Generated: October 31, 2026
2-Methoxyaniline → HCID 24985363, compound
https://huagongshe.com/reaction/388101
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methoxyaniline | HCID 7000 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2,6-Dichloro-3-nitropyridine | HCID 85239 | — |
| Reactant | HCID 2842435 | HCID 2842435 | — |
| Product | HCID 24985363 | HCID 24985363 | 81% |
Reaction Steps
6-Chloro-N-(2-methoxyphenyl)-3-nitropyridin-2-amine. 2,6-Dichloro-3-nitropyridine (3.0 g, 15.54 mmol) was dissolved in tetrahydrofuran (50 mL) and cooled to −78° C. A solution of o-anisidine (1.91 g, 15.54 mmol) and diisopropylamine (2.10 g, 16.31 mmol) in tetrahydrofuran (5 mL) was added dropwise. The mixture was stirred at ambient temperature for 16 h. The solution was condensed under reduced pressure and partitioned between water and ethyl acetate (3×), organics were pooled and dried over magnesium sulfate, filtered and solvent removed under reduced pressure to give the crude product. The solid was triturated with ethyl acetate/hexanes and the resultant precipitate filtered to afford the title compound (3.53 g, 81%). MS (ESI) m/z 280.1 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08372976B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-6e10736223f54c0caa212308179fc9b3 |
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| Source note | uspto-grants-2013_02 |
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