HRID45797

反应详情

EQUATION

反应方程式

HRID 45797 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a solution of tert-butyl 4-[(3-carbamoyl-8-iodo-4,5-dihydro-1H-pyrazolo[4,3-h]quinazolin-1-yl)methyl]piperidine-1-carboxylate (30 mg, 0.036 mmol) in 3 ml of 1,4-dioxane and 1 ml of water, under argon atmosphere, 17.6 mg (0.11 mmol) of 2,6-difluorophenylboronic acid 13.7 mg (0.017 mmol) of 1,1′-bis(diphenylphosphino)ferrocenepalladium complex with dichloromethane and 54 mg (0.167 mmol) of cesium carbonate, were successively added. The mixture was submitted to microwave irradiation at 80° for 1 hour in a sealed vial. The reaction was filtered through a celite pad and the solvent evaporated to dryness. The crude was then portioned between ethyl acetate and water, the organic layer dried over sodium sulphate and the solvent removed in vacuo. After purification by flash chromatography on silica gel column (DCM/EtOAc 7/3), 20 mg (70%) of tert-butyl 4-{[3-carbamoyl-8-(2,6-difluorophenyl)-4,5-dihydro-1H-pyrazolo[4,3-h]quinazolin-1-yl]methyl}piperidine-1-carboxylate were obtained. The product was dissolved in DCM (2 ml) and 4M HCl in 1,4-dioxane (2 ml) was added. The reaction was stirred at room temperature for 1 hour, the solvent was evaporated to dryness. The solid was treated with ethyl ether and the precipitate collected by filtration to give the title compound as a pale yellow solid 17 mg (85%). LC/MS (254 nm) HPLC method 2 Rt 4.14 min. 1H NMR (401 MHz, DMSO-d6) δ 8.89 (s, 1H), 8.57 (d, J=9.76 Hz, 1H), 8.30 (d, J=10.01 Hz, 1H), 7.55-7.69 (m, 1H), 7.45 (s, 1H), 7.37 (s, 1H), 7.23-7.33 (m, 2H), 4.57-4.66 (m, 2H), 3.16-3.26 (m, 2H), 3.01-3.14 (m, 4H), 2.69-2.85 (m, J=10.74 Hz, 2H), 2.09-2.29 (m, J=7.20 Hz, 1H), 1.56-1.70 (m, J=12.94 Hz, 2H), 1.32-1.48 (m, 2H) HRMS (ESI) calcd for C21H27IN6O3 [M+H]+ 425.1896 found 425.1896

WORKUP

后处理

  1. customirradiation at 80° for 1 hour in a sealed vial
  2. filtrationThe reaction was filtered through a celite pad
  3. customthe solvent evaporated to dryness
  4. dry with materialthe organic layer dried over sodium sulphate
  5. customthe solvent removed in vacuo
  6. customAfter purification by flash chromatography on silica gel column (DCM/EtOAc 7/3)