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
CONDITIONS
反应条件
- 温度
- 80 °C
PROCEDURE
实验过程
A 3 L round bottomed flask was charged with ethyl 3-(dimethylamino)-2-(4-nitrobenzoyl)acrylate (63.59 g, 217.5 mmol) and 2-aminomalonamide (33.12 g, 282.8 mmol) and AcOH (800 mL). The reaction mixture was heated to 80° C. over night. The starting material appeared consumed by TLC. The AcOH was removed under reduced pressure and TFA (400 mL) was added. The mixture was heated over night at 60° C. The reaction was cooled to room temperature and the TFA was removed under reduced pressure. The orange oil was washed with saturated aqueous NaHCO3 (1 L) and solid NaHCO3 was added until the solution was neutral. The solids were filtered and placed in a 1 L erlenmeyer flask. The solids were washed with H2O (3×1 L) and the water was decanted off through the filter. On the last washing the solids were poured onto the filter and allowed to air dry. The solids were once again removed from the filter and washed with Et2O (4×500 mL). The Et2O was decanted off through the filter and on the final washing the solids were transferred to the filter. An addition portion of Et2O (200 mL) was used to wash the flask and the filter cake. The product was dried in a vacuum oven at 40° C. over P2O5 for 4 h affording ethyl 5-(aminocarbonyl)-4-(4-nitrophenyl)-1H-pyrrole-3-carboxylate as a tan solid (55.2 g, 182 mmol, 83.7%). 1H-NMR (DMSO-d6) δ 12.33 (br s, 1H), 8.19-8.15 (m, 2H), 7.57 (d, J=3.6 Hz, 1H), 7.53-7.49 (m, 2H), 7.29 (br s, 1H), 6.41 (br s, 1H), 3.99 (q, J=7.2 Hz, 2H), 1.03 (t, J=7.2 Hz, 3H); LCMS RT=2.79 min; MS {M+H]+=304.2.
WORKUP
后处理
- customThe starting material appeared consumed by TLC
- customThe AcOH was removed under reduced pressure and TFA (400 mL)
- additionwas added
- temperatureThe mixture was heated over night at 60° C
- temperatureThe reaction was cooled to room temperature
- customthe TFA was removed under reduced pressure
- washThe orange oil was washed with saturated aqueous NaHCO3 (1 L) and solid NaHCO3
- additionwas added until the solution
- filtrationThe solids were filtered
- customplaced in a 1 L erlenmeyer flask
- washThe solids were washed with H2O (3×1 L)
- customthe water was decanted off through the filter
- washOn the last washing the solids
- additionwere poured onto the
- filtrationfilter
- customto air dry
- customThe solids were once again removed from the
- filtrationfilter
- washwashed with Et2O (4×500 mL)
- customThe Et2O was decanted off through the
- filtrationfilter
- washon the final washing the solids
- washto wash the flask
- dry with materialThe product was dried in a vacuum oven at 40° C. over P2O5 for 4 h