HRID908398

反应详情

EQUATION

反应方程式

HRID 908398 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A suspension of 3-(1,3-benzoxazol-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine (0.3 g), tert-butyl 4-(4-bromo-3-formyl-pyrazol-1-yl)piperidine-1-carboxylate (0.362 g), potassium carbonate (0.335 g) and tetrakis(triphenylphosphine) palladium (0.093 g) in degassed acetonitrile (50 mL) was stirred at reflux overnight. The resulting suspension was cooled to ambient temperature, filtered, washed with dichloromethane (3×20 ml) and the filtrate was concentrated. The crude product was purified by flash chromatography on silica gel eluting with 5 to 90% ethyl acetate in petroleum ether. The solvent was evaporated to dryness to afford tert-butyl 4-[4-[6-amino-5-(1,3-benzoxazol-2-yl)-3-pyridyl]-3-formyl-pyrazol-1-yl]piperidine-1-carboxylate (0.370 g) as a solid. NMR Spectrum: (DMSOd6) 1.44 (s, 9H), 1.87 (dd, 1H), 1.92 (dd, 1H), 2.09-2.18 (m, 2H), 2.97 (bs, 2H), 4.04-4.16 (m, 2H), 4.52-4.61 (m, 1H), 7.41-7.49 (m, 2H), 7.80 (dd, 1H), 7.82 (bs, 2H), 7.85 (dd, 1H), 8.48 (s, 1H), 8.56 (d, 1H), 8.65 (d, 1H), 9.99 (s, 1H); Mass spectrum: M+H+ 489.

WORKUP

后处理

  1. temperatureat reflux overnight
  2. filtrationfiltered
  3. washwashed with dichloromethane (3×20 ml)
  4. concentrationthe filtrate was concentrated
  5. customThe crude product was purified by flash chromatography on silica gel eluting with 5 to 90% ethyl acetate in petroleum ether
  6. customThe solvent was evaporated to dryness