D(-)-Leucinol → (R)-4-[5-Phenylmethylthio-7-(1-hydroxymethyl-3-methyl-butylamino)-thiazolo[4,5-d]pyrimidin-2-ylamino]-piperidine-1-carboxylic acid tert-butyl ester

참여 물질

반응 조건

반응 단계

The product from step (a) (50 mg, 0.1 mmol) and D-leucinol (60 mg, 0.5 mmol) were dissolved in anhydrous tetrahydrofuran (3 mL). The solution was heated in a capped reaction tube at 100° C. for 7 days. The crude product was flash chromatographed on silica (gradient eluent—ammonia:ethyl acetate:chloroform, 1:9:90 to 1:49:50). The product was dried in vacuo at room temperature resulting in 44 mg (76% yield) of the title compound as a white solid.

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