反应详情

温度

25 °C

[7-(Methanesulfonylamino-methyl)-1,1-dioxo-1,4-dihydro-1λ6-thieno[2,3-e][1,2,4]thiadiazin-3-yl]-acetic acid (prepared as described in Example 2c; 0.148 g, 0.419 mmol), O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (0.175 g, 0.460 mmol) and 4-methylmorpholine (0.092 mL, 0.837 mmol) were added sequentially to a solution of rac-2-cyclopropylaminomethyl-2,5-dimethyl-hexanoic acid ethyl ester (0.101 g, 0.418 mmol) in N,N-dimethylformamide (6 mL) at 25° C. The reaction mixture was stirred at 25° C. for 20 h, and then was concentrated in vacuo. The residue was partitioned between 1.0 M aqueous hydrochloric acid solution (100 mL) and ethyl acetate (2×100 mL). The organic layers were dried over sodium sulfate and were concentrated in vacuo. The residue was dissolved in ethanol (12 mL) at 25° C. A 21 wt. % solution of sodium ethoxide in ethanol (0.813 mL, 2.51 mmol) was added and the reaction mixture was heated to 70° C. for 26 h. After cooling to 25° C., the reaction mixture was partitioned between 1.0 M aqueous hydrochloric acid solution (150 mL) and ethyl acetate (2×150 mL). The organic layers were dried over sodium sulfate and were concentrated in vacuo. The residue was purified by flash chromatography (Teledyne Isco RediSep column; 50-100% ethyl acetate in hexanes) to afford rac-N-{3-[1-Cyclopropyl-4-hydroxy-5-methyl-5-(3-methyl-butyl)-2-oxo-1,2,5,6-tetrahydro-pyridin-3-yl]-1,1-dioxo-1,4-dihydro-1λ6-thieno[2,3-e][1,2,4]thiadiazin-7-ylmethyl}-methanesulfonamide (0.109 g, 0.205 mmol, 49%) as an orange oil. 1H NMR (400 MHz, DMSO-d6) δ: 0.70 (4H, bs), 0.84-0.86 (6H, m), 1.09 (3H, s), 1.12-1.15 (2H, m), 1.50 (2H, bs), 2.81 (1H, bs), 2.95 (3H, s), 3.27 (1H, d, J=13.5 Hz), 4.23 (2H, d, J=5.4 Hz), 7.26 (1H, s), 7.65 (1H, t, J=6.2 Hz). LC-MS (ESI) calculated for C21H30N4O6S3 530.13. found 531.0 [M+H+].

1. concentrationwas concentrated in vacuo
2. customThe residue was partitioned between 1.0 M aqueous hydrochloric acid solution (100 mL) and ethyl acetate (2×100 mL)
3. dry with materialThe organic layers were dried over sodium sulfate
4. concentrationwere concentrated in vacuo
5. dissolutionThe residue was dissolved in ethanol (12 mL) at 25° C
6. temperaturethe reaction mixture was heated to 70° C. for 26 h
7. temperatureAfter cooling to 25° C.
8. customthe reaction mixture was partitioned between 1.0 M aqueous hydrochloric acid solution (150 mL) and ethyl acetate (2×150 mL)
9. dry with materialThe organic layers were dried over sodium sulfate
10. concentrationwere concentrated in vacuo
11. customThe residue was purified by flash chromatography (Teledyne Isco RediSep column; 50-100% ethyl acetate in hexanes)