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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603549Generated: October 29, 2026

Methylamine → (4-Benzenesulphonyl-6-bromopyridin-2-yl)-methylamine

https://huagongshe.com/reaction/1603549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant4-Benzenesulphonyl-2,6-dibromopyridineHCID 54112330—
SolventEthanolHCID 702—
Solvent1,4-DioxaneHCID 31275—
Product(4-Benzenesulphonyl-6-bromopyridin-2-yl)-methylamineHCID 1541039761%

Reaction Steps

0.42 g (0.00112 mol) of 4-benzenesulphonyl-2,6-dibromopyridine and 1.4 ml of 8M methylamine in ethanol were stirred at room temperature in a mixture of 11 ml of ethanol and 11 ml of dioxane for 48 hrs. After removal of the solvent the residue was chromatographed on silica gel with ethyl acetate/hexane 1:10. The product-containing fractions were suspended in 25 ml of diethyl ether, treated in an ultrasound bath and diluted with 45 ml of hexane. The suspension was suction filtered and the filter material was dried in a high vacuum. There was obtained 0.224 g (61%) of (4-benzenesulphonyl-6-bromopyridin-2-yl)-methylamine as white crystals; m.p.: 145-148° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990105
Source datasetuspto-grants-1999_11
ORD IDord-5e5ad1c6e525466d9b5a1d3fe4fcec69
Source noteuspto-grants-1999_11