HRID2258546
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
A mixture of 1.5 g of the compound obtained in Example 15 Step B, 1 g of 2-dimethylamino-1,1-dimethylethylamine (synthesized according to J. Am. Chem. Soc., 1946, 68, 12-14), 1.6 g of BOP and 2 g of DIPEA in 20 ml of DCM is left stirring for 1 hour at RT. The reaction mixture is concentrated under vacuum, the residue is extracted with EtOAc, the organic phase is washed with 1N NaOH solution, with water and dried over Na2SO4, and the solvent is evaporated off under vacuum. The residue is chromatographed on silica, eluting with a DCM/MeOH mixture (98/2; v/v). 0.15 g of the expected product is obtained after crystallization from iso ether, mp=161° C.
WORKUP
后处理
- waitis left
- concentrationThe reaction mixture is concentrated under vacuum
- extractionthe residue is extracted with EtOAc
- washthe organic phase is washed with 1N NaOH solution, with water
- dry with materialdried over Na2SO4
- customthe solvent is evaporated off under vacuum
- customThe residue is chromatographed on silica
- washeluting with a DCM/MeOH mixture (98/2; v/v)