반응 #47377

ord-8b5d329d074e4049914e0c2fad32866e

반응 조건

온도
25°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwas added
  2. 2
    세척The mixture was washed with saturated ammonium chloride (1 mL)
  3. 3
    기타evaporated
  4. 4
    기타the crude product purified by HPLC (Gilson semi-prep; Supelcosil ABZ+Plus 12 μM 25 cm×21.2 mm column 20-95% acetonitrile/water gradient) which

실험 절차

To a solution of (S)-2-[4-(2-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid (prepared as in Example 64, 68 mg, 0.21 mmol) in dichloromethane (1.00 mL) was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (45 mg, 0.23 mmol) and 1-hydroxybenzotriazole (30 mg, 0.22 mmol). The resulting solution was stirred for 5 min before 3-(3,3,3-trifluoro-propyl)-[1,2,4]thiadiazol-5-ylamine (50 mg, 0.25 mmol) was added and the resulting mixture stirred at 25° C. overnight. The mixture was washed with saturated ammonium chloride (1 mL), evaporated and the crude product purified by HPLC (Gilson semi-prep; Supelcosil ABZ+Plus 12 μM 25 cm×21.2 mm column 20-95% acetonitrile/water gradient) which afforded (S)-2-[4-(2-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid [3-(3,3,3-trifluoro-propyl)-[1,2,4]thiadiazol-5-yl]-amide (52 mg, 49%) as a light yellow solid: HR-ES-MS m/z calculated for C21H22ClF3N4O3S [M+H]+ 503.1126, observed 503.1127; 1H NMR (300 MHz, DMSO-d6) δ ppm 0.92 (d, J=6.6 Hz, 3H), 0.95 (d, J=6.6 Hz, 3H), 1.48 (br. s., 1H), 1.55-1.77 (m, 1H), 1.77-1.97 (m, 1H), 2.66-2.90 (m, 2H), 3.05 (t, J=6.9 Hz, 2H), 4.30 (d, J=18.4 Hz, 1H), 4.51 (d, J=18.4 Hz, 1H), 4.83 (s, 1H), 4.93-5.07 (m, 1H), 7.37 (td, J=8.0, 1.5 Hz, 1H), 7.47 (td, J=8.0, 1.5 Hz, 1H), 7.54 (dd, J=8.0, 1.2 Hz, 1H), 7.66 (dd, J=8.0, 1.2 Hz, 1H), 13.38 (s, 1H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07741327B2uspto-grants-2010_06