反应详情

温度

60 °C

In 100 mL of acetonitrile was added sodium thioisocyanate (1.5 g, 20 mmol), pyridine (3.5 g, 44 mmol), followed by (R)-N-(methylsulfonyloxy)-1,4-dioxaspiro[4.5]decane-2-carbimidoyl chloride (5.2 g, 18 mmol) and the reaction heated to 60° C. for 30 minutes. 5-Bromo-3-(2-methylpyridin-3-yloxy)pyridin-2-amine (4.1 g, 15 mmol) was added and the reaction was heated overnight at 60° C. The reaction was concentrated to one quarter volume and the residue was partitioned between EtOAc and water made basic with 1N NaOH. The combined organic layers were separated and the aqueous layer extracted with EtOAc. The combined organic layers were washed with brine, dried over MgSO4 and concentrated in vacuo. The material was purified on silica gel (25% EtOAc in CH2Cl2) to afford (S)-N-(5-bromo-3-(2-methylpyridin-3-yloxy)pyridin-2-yl)-3-(1,4-dioxaspiro[4.5]decan-2-yl)-1,2,4-thiadiazol-5-amine (5.4 g, 73%).

1. temperaturethe reaction was heated overnight at 60° C
2. concentrationThe reaction was concentrated to one quarter volume
3. customthe residue was partitioned between EtOAc and water
4. customThe combined organic layers were separated
5. extractionthe aqueous layer extracted with EtOAc
6. washThe combined organic layers were washed with brine
7. dry with materialdried over MgSO4
8. concentrationconcentrated in vacuo
9. customThe material was purified on silica gel (25% EtOAc in CH2Cl2)