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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603550Generated: October 31, 2026

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

https://huagongshe.com/reaction/1603550

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Benzenesulphonyl-6-bromopyridin-2-yl)-methylamineHCID 15410397—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product(4-Benzenesulphonylpyridin-2-yl)-methylamineHCID 1541039837%

Reaction Steps

0.09 g (0.000275 mol) of (4-benzenesulphonyl-6-bromopyridin-2-yl)-methylamine was dissolved in 7 ml of ethanol, treated with 0.009 g of Pd/C (10%) and hydrogenated under normal pressure for 18 hrs. Thereafter, the catalyst was filtered off, the solvent was removed and the residue was partitioned in ethyl acetate and saturated bicarbonate solution. The organic phase was washed with sat. sodium chloride solution and dried over MgSO4. After removal of the solvent the residue was chromatographed on silica gel with ethyl acetate/hexane 1:4 and 1:3. There was obtained 0.025 g (37%) of (4-benzenesulphonylpyridin-2-yl)-methylamine as beige crystals; m.p.: 142-143° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990105
Source datasetuspto-grants-1999_11
ORD IDord-512af824325540de941a68cc448b03dc
Source noteuspto-grants-1999_11