反应详情

In a manner similar to that described for Example 1, method A, the title compound (3.53 g, 46%) was prepared from malonic acid monoallyl ester (2.88 g, 20 mmol) and 6-aminopenicillanic acid (4.33 g, 20 mmol) as colorless crystals: m.p. 59°-60° C. (toluene); IR (CHCl3) 1790, 1730, 1685 cm-1; 1 H NMR (CDCl3) δ 1.51 and 1.67 (each 3H, s, C2 -(CH3)2), 3.35-3.47 (2H, m, COCH2CO), 4.48 (1H, s, C3 -H), 4.60-4.70 (4H, m, 2xOCH2CH=CH2), 5.22-5.42 (4H, m, 2xOCH2CH=CH2), 5.56 (1H, d, J=4Hz, C5-H), 5.75 (1H, dd, J=4 and 9Hz, C6 -H), 5.84-6.00 (2H, m, 2xOCH2CH=CH2), 8.03 (1H, d, J=9Hz, NH).