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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796327Generated: November 1, 2026

2,4,6-Trimethylaniline → N-mesityl-3-(4-methoxyphenylsulfonyl)-6-methylpyridin-2-amine

https://huagongshe.com/reaction/1796327

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrimethylanilineHCID 6913—
Reactant2-Chloro-3-(4-methoxybenzenesulfonyl)-6-methylpyridineHCID 22181677—
SolventEthylene GlycolHCID 174—
ProductN-mesityl-3-(4-methoxyphenylsulfonyl)-6-methylpyridin-2-amineHCID 1147495965.5%

Reaction Steps

2-chloro-3-(4-methoxybenzenesulfonyl)-6-methylpyridine (1.6 g, 5.39 mmol) and 2,4,6-trimethylaniline (4.4 g, 32.8 mmol) were heated at reflux in ethylene glycol (5.5 mL) for 20 h. After cooling, the reaction was partitioned between EtOAc (100 mL) and 0.5 N NaOH (20 mL) and the aqueous layer was extracted with EtOAc (100 mL) and the combined organic extracts were washed with water, brine, dried and stripped in vacuo. The residue was chromatographed on silica gel using 20% EtOAc/hexanes as eluent to give [3-(4-methoxybenzenesulfonyl)-6-methyl-pyridin-2-yl]-(2,4,6-trimethylphenyl)-amine as a solid (1.4 g), mp 165–167° C. mass spec. (AP+): m/z 397 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030145B2
Source datasetuspto-grants-2006_04
ORD IDord-fdc831fb07a84cea93bb198a1a80acbd
Source noteuspto-grants-2006_04