反应详情

To a mixture of (S)-6-(1-(tert-butoxy)-2-ethoxy-2-oxoethyl)-7-(4,4-dimethylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidine-2-carboxylic acid (50 mg, 0.112 mmol) and 3,3-dimethylbutan-1-amine (22.66 mg, 0.224 mmol) in DMF (2 mL) was added DIEA (0.098 mL, 0.560 mmol), HATU (85 mg, 0.224 mmol) and DMAP (2.74 mg, 0.022 mmol) and the resulting mixture was stirred at room temp for 16 h. At this point LCMS indicated completion of reaction. Water was then added and the mixture was extracted with ethyl acetate (25 mL), washed with brine (15 mL), dried (Na2SO4), filtered and concentrated. Crude was then treated with 1N NaOH (0.336 mL, 0.336 mmol) in MeOH (2.000 mL) at 60° C. for 5 h. Mixture was then cooled and purified by prep-HPLC to afford (S)-2-(tert-butoxy)-2-(2-((3,3-dimethylbutyl)carbamoyl)-7-(4,4-dimethylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)acetic acid (41.6 mg, 0.079 mmol, 70.4% yield). 1H NMR (500 MHz, DMSO-d6) δ 8.13 (t, J=5.6 Hz, 1H), 6.77 (s, 1H), 5.46 (s, 1H), 3.37-3.28 (m, 6H), 1.92 (s, 3H), 1.67-1.55 (m, 2H), 1.54-1.40 (m, 4H), 1.14 (s, 9H), 1.08 (br. s., 6H), 0.96 (s, 9H). LCMS (M+H)=502.5.

1. customcompletion of reaction
2. extractionthe mixture was extracted with ethyl acetate (25 mL)
3. washwashed with brine (15 mL)
4. dry with materialdried (Na2SO4)
5. filtrationfiltered
6. concentrationconcentrated
7. temperatureMixture was then cooled
8. custompurified by prep-HPLC