تفاعل #70592

ord-aeb70ef3f1d54c829010830539e88f70

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىEthanol was removed under reduced pressure
  2. 2
    workup.ADDITIONthe solution diluted with water
  3. 3
    استخلاصsubsequently extracted with diethyl ether (2×30 mL)
  4. 4
    ترشيحThe solid precipitate was filtered
  5. 5
    غسيلwashed with water
  6. 6
    أخرىdried under high vacuum

الإجراء التجريبي

To a solution consisting of lithium hydroxide monohydrate (0.38 g, 9.0 mmol) dissolved in ethanol (20 mL)/water (10 mL) was added tert-butyl 2-(2-phenylpyrimidin-5-yl)thiazole-4-carboxylate (Example 62, 705 mg, 3.0 mmol) in dry DMF (11 mL) and the mixture stirred at room temperature for 18 hours. Ethanol was removed under reduced pressure and the solution diluted with water and subsequently extracted with diethyl ether (2×30 mL). The aqueous phase was acidified with 2 N hydrochloric acid to pH2. The solid precipitate was filtered, washed with water and dried under high vacuum to give the title compound as an off-white solid (371 mg, 87% yield); Rf 0.15 with 9:1 v/v dichloromethane-methanol; 1H-NMR (300 MHz; DMSO-d6) δ 9.39 (s, 2H), 8.63 (s, 1H), 8.44 (dd, 2H), 7.55 (m, 3H); MS (ESI+) m/z 284 (M+1); H-PGDS FPBA IC50: 1.1 μM.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08536185B2uspto-grants-2013_09