反应详情

Tris(1,1-dimethylethyl)2-(2,6-dichloro-5-fluoro-4-pyrimidinyl)-1,1,2-hydrazinetricarboxylate (0.988 g, 1.992 mmol) was dissolved in THF (10 mL). To this solution was added triethylamine (0.61 mL, 4.3765 mmol), followed by commercially available 2-aminomethyl thiazole hydrochloride (0.30 g, 1.992 mmol), which was suspended in THF (12 mL). The reaction was left to stir for 2 days during which time an additional 10 mL THF and 2-aminomethyl thiazole hydrochloride (0.061 g, 0.4049 mmol) were added to the reaction mixture. After 3 more days, the reaction mixture was diluted with water and extracted with ethyl acetate. The organics were dried (Na2SO4) and concentrated. The resulting crude material was purified by silica gel chromatography (0-100% ethyl acetate in hexanes) to provide tris(1,1-dimethylethyl)2-{2-chloro-5-fluoro-6-[(1,3-thiazol-2-ylmethyl)amino]-4-pyrimidinyl}-1,1,2-hydrazinetricarboxylate as a yellow oil (0.5826, 51%). LCMS: (M+H−3 Boc)+=375.0.

1. waitThe reaction was left
2. additionwere added to the reaction mixture
3. extractionextracted with ethyl acetate
4. dry with materialThe organics were dried (Na2SO4)
5. concentrationconcentrated
6. customThe resulting crude material was purified by silica gel chromatography (0-100% ethyl acetate in hexanes)