反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
产物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 100 °C
PROCEDURE
实验过程
To a mixture of [1-(5-iodo-pyridin-2-yl)-cyclopropyl]-carbamic acid tert-butyl ester (500 mg, 1.39 mmol), 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole 433 mg, 2.1 mmol) and Pd(dppf)Cl2.dichloromethane complex (113 mg, 0.14 mmol) in 1.5 mL of DME/H2O/EtOH (7:3:2) in a sealable microwave tube was added 1M aqueous K3PO4 solution (2.1 mL). The tube was sealed and heated in the microwave at 100° C. for 10 min. The crude reaction was filtered through a pad of silica gel, washing with MeOH, and concentrated. The residue was partitioned between 30 mL of EtOAc and 10 mL of water. The organic phase was washed with brine, dried over Na2SO4, filtered, and concentrated to give an oil. This material was purified by normal phase flash chromatography on silica gel (0→3.5% MeOH/CH2Cl2) to give 0.55 g of {1-[5-(1-methyl-1H-pyrazol-4-yl)-pyridin-2-yl]-cyclopropyl}-carbamic acid tert-butyl ester as a brown solid. The compound was used in subsequent steps without further purification.
WORKUP
后处理
- customThe tube was sealed
- customThe crude reaction
- filtrationwas filtered through a pad of silica gel
- washwashing with MeOH
- concentrationconcentrated
- customThe residue was partitioned between 30 mL of EtOAc and 10 mL of water
- washThe organic phase was washed with brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customto give an oil
- customThis material was purified by normal phase flash chromatography on silica gel (0→3.5% MeOH/CH2Cl2)