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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177251Generated: October 25, 2026

2-Amino-5-methylpyridine → 2-Methyl-N-(5-methylpyridin-2-yl)-4-(4-(methylsulfonyl)-phenoxy)-benzofuran-6-carboxamide

https://huagongshe.com/reaction/1177251

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-methylpyridineHCID 15348—
ReactantChlorodimethylaluminumHCID 79147—
ReactantEthyl 2-methyl-4-(4-(methylsulfonyl)phenoxy)benzofuran-6-carboxylateHCID 59560179—
Solvent1,2-DichloroethaneHCID 11—
Product2-Methyl-N-(5-methylpyridin-2-yl)-4-(4-(methylsulfonyl)-phenoxy)-benzofuran-6-carboxamideHCID 6675586986%

Reaction Steps

2-Amino-5-methylpyridine (289 mg, 2.67 mmol) was dissolved in DCE (10 mL) at 0° C., then Al(CH3)2Cl (2.67 mL, 1M in hexanes) was added drop wise. After the addition, the ice-bath was removed, and the mixture was stirred for 30 min at room temperature. Ethyl 2-methyl-4-[4-(methylsulfonyl)phenoxy]-1-benzofuran-6-carboxylate (100 mg, 0.267 mmol) was added and the stirring was continued for 14 h. The reaction was quenched with potassium sodium tartrate tetrahydrate (20% w/w) cautiously. The product was extracted with CHCl3, washed with brine and dried over MgSO4. The crude product was purified by gradient silica gel chromatography using CHCl3/MeOH (100/0 to 98/2) to give the title compound (100 mg, 86%) as a white solid. 1H NMR (300 MHz, CHLOROFORM-D) δ ppm 2.32 (s, 3 H) 2.48 (s, 3 H) 3.07 (s, 3 H) 6.24 (s, 1 H) 7.08-7.16 (m, 2 H) 7.48 (d, J=1.32 Hz, 1 H) 7.57 (dd, J=8.29, 2.35 Hz, 1 H) 7.81-7.97 (m, 3 H) 8.12 (d, J=2.35 Hz, 1 H) 8.25 (d, J=8.29 Hz, 1 H) 8.44 (s, 1 H). LCMS for C23H20N2O5S m/z 437.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842713B2
Source datasetuspto-grants-2010_11
ORD IDord-dfb079e543c143949e7f875de7ce5c4a
Source noteuspto-grants-2010_11