反应详情

To a cooled solution (−70° C.) of (2R)-3,6-dimethoxy-2-(propan-2-yl)-2,5-dihydropyrazine (25.8 g, 140 mmol, 2 eq.) in tetrahydrofuran (200 mL) was added dropwise n-butyllithium (2.5 M, 64.4 mL, 161 mmol 2.3 eq.) and then stirred for 30 minutes. A solution of #210 (15.4 g, 70 mmol, 1 eq.) in tetrahydrofuran (150 mL) was added dropwise at −65° C. and then the solution was stirred for 2 hours at this temperature. The reaction was quenched by saturated aqueous ammonium chloride (100 mL) and extracted with ethyl acetate (100 mL). The organic phase was dried over sodium sulfate and concentrated in vacuo. The residue was purified by silica column chromatography (Gradient: 10 to 16% ethyl acetate in petroleum ether) to afford #211 (7.3 g, 32%, over two steps) as yellow solid. LC-MS (Protocol Z): m/z 326.2 [M+H+], retention time=0.88 minutes.

1. stirringthe solution was stirred for 2 hours at this temperature
2. customThe reaction was quenched by saturated aqueous ammonium chloride (100 mL)
3. extractionextracted with ethyl acetate (100 mL)
4. dry with materialThe organic phase was dried over sodium sulfate
5. concentrationconcentrated in vacuo
6. customThe residue was purified by silica column chromatography (Gradient: 10 to 16% ethyl acetate in petroleum ether)
7. customto afford #211 (7.3 g, 32%, over two steps) as yellow solid