反应详情

Combine (1H-benzimidazol-2-yl)-(1-ethoxycarbonyl-piperidin-4-yl)amine (1.5 g, 5.2 mmol) in tetrahydrofuran (45 mL) and dimethylformamide (5 mL). Cool in an ice-bath. Add sodium hydride (0.25 g, 60% n in oil, 6.24 mmol). After 90 minutes, add 2-(chloromethyl)furan (0.90 g, 7.8 mmol). Warm to ambient temperature. After 60 hours, quench by the addition of ice and then a saturated aqueous ammonium chloride solution. Evaporate to remove most of the tetrahydrofuran, dilute with ethyl acetate, and extract with a saturated aqueous sodium bicarbonate solution, water, and then brine. Dry the organic layer over MgSO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with ethyl acetate to give (1-(fur-2-ylmethyl)-1H-benzimidazol-2-yl)(1-(ethoxycarbonyl)piperidin-4-yl)amine: Rf=0.29 (silica gel, ethyl acetate).

1. temperatureCool in an ice-bath
2. waitAfter 60 hours
3. customquench by the addition of ice
4. customEvaporate
5. customto remove most of the tetrahydrofuran
6. additiondilute with ethyl acetate
7. extractionextract with a saturated aqueous sodium bicarbonate solution, water
8. dry with materialDry the organic layer over MgSO4
9. filtrationfilter
10. customevaporate in vacuo
11. customto give a residue