(5BETA,17BETA)-17-羟基-17-(甲基-D3)-2'H-雄甾-2-烯并[3,2-C]吡唑-5'(1'H)-酮 → 克拉维酸钾

参与物

反应步骤

Lithium clavulanate (5.6 gm, estimated purity 88.8% pfa 0.025 M) was dissolved in water (45 mls) and the resulting pale-red-brown solution was cooled in an ice bath. Tripotassium orthophosphate (10.1 mls of 1 M solution, 1.2 equivalents) was added in one lot and methanol (18 mls) added over 1/2 hr with a small quantity of lithium phosphate (ca. 1 mg) for seeding. As lithium phosphate separated out the pH dropped from 8.7 to about 7.5. Acetone was added over 3/4 hr to 800 mls. The material that separated out was quite orange-brown at this point and the supernatant a very pale yellow. Celite (2 g) filtration gave a clear solution which was added to acetone (1750 mls) with vigorous stirring over 1 hr. The white solid was filtered off leaving a very pale yellow filtrate. Washing with acetone (3×50 ml) and fluid bed drying gave potassium clavulanate (4.1 g, 84% pfa, 69% recovery).

来源与证据