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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388101Generated: October 31, 2026

2-Methoxyaniline → HCID 24985363, compound

https://huagongshe.com/reaction/388101

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyanilineHCID 7000—
ReactantDiisopropylamineHCID 7912—
ReactantTetrahydrofuranHCID 8028—
Reactant2,6-Dichloro-3-nitropyridineHCID 85239—
ReactantHCID 2842435HCID 2842435—
ProductHCID 24985363HCID 2498536381%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372976B2
Source datasetuspto-grants-2013_02
ORD IDord-6e10736223f54c0caa212308179fc9b3
Source noteuspto-grants-2013_02