反応 #60911
ord-91338da205db4600923c3a2fc907939b
反応方程式
6-[4-(3-Iodophenyl)-1-methyl-1H-imidazol-5-yl]thieno[2,3-d]pyrimidin-4-amine
tert-butyl carbamate
N,N′-dimethylethylenediamine
potassium phosphate
→
title compound
収率 9.5%
tert-Butyl {3-[5-(4-aminothieno[2,3-d]pyrimidin-6-yl)-1-methyl-1H-imidazol-4-yl]phenyl}carbamate
収率 9.5%
反応物
反応条件
温度
100°CELSIUS
詳細条件
See reaction.notes.procedure_details.
後処理
- 1その他degassed
- 2その他The mixture was partitioned between EtOAc and dilute aqueous NH3
- 3その他The organic phase was dried
- 4その他evaporated
- 5その他The residue was purified by flash chromatography on silica using a gradient of 0-100% EtOAc in DCM
- 6その他Fractions were evaporated
実験手順
6-[4-(3-Iodophenyl)-1-methyl-1H-imidazol-5-yl]thieno[2,3-d]pyrimidin-4-amine (Example 49) (43 mg) was stirred with tert-butyl carbamate (24 mg), N,N′-dimethylethylenediamine (9 mg), copper(I) iodide (10 mg), and potassium phosphate (42 mg) in 1,4-dioxane (2 mL), degassed, and heated under an inert atmosphere at 100° C. for 24 hours. The mixture was partitioned between EtOAc and dilute aqueous NH3. The organic phase was dried and evaporated. The residue was purified by flash chromatography on silica using a gradient of 0-100% EtOAc in DCM then 0-20% MeOH in DCM as eluent. Fractions were evaporated to give the title compound as a gum (4 mg, 9%);