反应详情

温度

0 °C

An oven dried flask was charged with 6-(tert-butyl-dimethyl-silanyloxymethyl)-pyridin-2-ylamine (1.27 g, 5.33 mmol) and 10 mL anhydrous THF. The solution was cooled to 0° C. and NaH (60% dispersion, 0.43 g, 11 mmol) was added. The reaction was warmed to room temperature and 2-chloro-thiazole-5-carbonitrile (0.924 g, 6.39 mmol) was added. The reaction was heated to 50° C. for 4 h. An additional 0.200 g (1.38 mmol) 2-chloro-thiazole-5-carbonitrile was added and the reaction was heated overnight. After a total of 18 h the reaction was cooled and quenched with water. The pH was adjusted to 7 with 1M HCl. The resulting precipitate was filtered and washed with water. Purification in two batches by flash column chromatography (suspended material on 5g silica, eluted DCM to 97:3 DCM/MeOH) afforded a mixture of the aminothiazole and starting aminopyridine. This aminothiazole (0.710 g, 2.05 mmol) was dissolved in 10 mL anhydrous THF and the resulting solution was cooled to 0° C. HF-pyr, 2.4 mL, was added and the reaction was allowed to warm to room temperature. After 1 h the reaction was quenched by the addition of sat NaHCO3 (aq) and the THF was removed in vacuo. The resulting precipitate was filtered and washed with water to provide the titled compound. 1H NMR (DMSO-d6) δ12.18 (s, 1H), 8.22 (s, 1H), 7.78 (t, 1H, J=7.6 Hz), 7.10 (d, 1H, J=7.5 Hz), 6.96 (d, 1H, J=8.2 Hz), 5.45 (t, 1H, J=5.7 Hz), 4.59 (d, 2H, J=5.9 Hz).

1. customAn oven dried flask
2. temperatureThe reaction was warmed to room temperature
3. temperatureThe reaction was heated to 50° C. for 4 h
4. temperaturethe reaction was heated overnight
5. temperatureAfter a total of 18 h the reaction was cooled
6. customquenched with water
7. filtrationThe resulting precipitate was filtered
8. washwashed with water
9. customPurification in two batches
10. washby flash column chromatography (suspended material on 5g silica, eluted DCM to 97:3 DCM/MeOH)
11. customafforded
12. temperaturethe resulting solution was cooled to 0° C
13. additionHF-pyr, 2.4 mL, was added
14. temperatureto warm to room temperature
15. customAfter 1 h the reaction was quenched by the addition of sat NaHCO3 (aq)
16. customthe THF was removed in vacuo
17. filtrationThe resulting precipitate was filtered
18. washwashed with water